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Systemadministratör till AVISEQ i Göteborg

Systemadministratör
Läs mer Jun 23
AVISEQ NMC, Network Management Center, är inne i ett intensivt utvecklingsskede och expanderar inom alla kategorier. Därför söker vi nu fler Systemadministratörer till vårt team. Vi gör nu en större satsning där vi fokuserar på att bygga upp en leveransförmåga inom området Infrastruktur innehållande datacenter, virtuella miljöer med RedHat OpenShift.

På AVISEQ arbetar vi med att bygga, utveckla och underhålla samhällskritiska system i utmanande och spännande miljöer. Du kommer in i ett härligt team där humor är lika självklart som kunskapsdelning och hjälpsamhet.


Om tjänsten
I rollen som Systemadministratör arbetar du både förvaltande i vår interna systemmiljö samt utvecklande tillsammans med våra kunder där du är med i hela processen från förstudie och analys till design, installation och drift av deras miljöer.

Dina arbetsuppgifter i huvudsak
• Arbete i kundrelaterade projekt med VMware-relaterade lösningar
• Teknisk konsultation i uppdrag mot kund, medverka vid kundmöten
• Tekniskt stöd för vår NOC (1st line – Network Operation Center)
• Utbilda kollegor vid behov
• Teknisk förvaltning av befintliga produkter

Du får arbeta på ett företag som är en ledare inom sin bransch och du blir en del av ett team som består av ambitiösa och engagerade kollegor. Som Systemadministratör får du chansen att vara med och påverka vår verksamhet och bidra till vår marknadsledande position.


Vem är du?
För att trivas med och lyckas i rollen som Systemadministratör på AVISEQ är du självständig och drivande men har samtidigt lätt för att samarbeta, både med kollegor och med våra kunder. Du är ansvarstagande och systematisk och gillar ordning och reda. Du har en kreativ och lösningsorienterad inställning till hur du utför ditt arbete och du har viljan att ständigt uppdatera dina kunskaper.

Vi ser gärna att du har minst 5 års erfarenhet av arbete med VMware (vSphere, vSAN), Linuxmiljö och Microsoft Server. Vi tror att du i botten har en högskoleutbildning med inriktning på IT. Du är flytande i svenska och engelska både i tal och skrift.
Du välkomnas till ett företag där det är högt i tak och där vi lägger stort värde i de personliga egenskaperna. Grundläggande kunskaper från RedHat (OpenShift), lagringslösningar, Active Directory, Microsoft och Scripting-erfarenhet är mycket meriterande.


Om verksamheten
AVISEQ verkar inom kritisk kommunikation. Vi är specialister på att erbjuda kostnadseffektiva tjänster utan att göra avkall på säkerheten. Vi övervakar, driftar och underhåller våra kunders tekniska utrustning och system, allt för att säkerställa deras kritiska verksamhet. Våra största kunder verkar inom luftfart och säkerhet vid flygtrafikcentraler, flygplatser, statliga myndigheter och företag, såväl offentliga som privata, i hela Sverige. AVISEQ har cirka 200 anställda och blev i maj 2020 en del av LFV-koncernen. Vi vill vara den bästa arbetsplatsen för dig som gillar utmaningar och att ta ett samhällsansvar!
Tjänsten är en tillsvidareanställning på 100%, där vi tillämpar 6 månaders provanställning. Grund för anställning är godkänd registerkontroll/säkerhetsprövning och tillträde sker enligt överenskommelse.

Urval sker löpande, så ansök nu.

För mer information besök gärna https://aviseq.se/

#LI-HG1

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Senior Scientist - Protein production & protein biochemistry

Forskare, farmakologi
Läs mer Jun 20
Are you truly passionate about the magic that happens in the lab and could see yourself applying your protein science knowledge in a successful pharmaceutical company? Would you like to join a team of highly skilled scientists where both your professional and personal skills are valued? If yes, this might be the spot for you!

We have an exciting opportunity for a Senior Scientist with protein science skills to join us, working within a dynamic scientific environment to support drug discovery. The Discovery Biology department within Discovery Sciences is responsible for the generation of novel reagents and assays to support projects in all phases of the drug discovery pipeline. We focus on scientific advances in small molecules, oligonucleotides and other new technologies and drug discovery platforms across our different core areas.

Thrive in a place where the brightest and most curious minds seamlessly come together in our inclusive environment.

Responsibilities
You will be responsible for producing and characterizing recombinant proteins including enzymes, secreted proteins, transcription factors and proteins with less characterized functions. These proteins are used to enable drug discovery projects. Since this position is lab based, we expect that you get a lot of energy from being in the lab and have a true real passion for practical duties. We also want you to contribute to our specific field developments in the team.

In the daily work, we rely on you to deliver expertise in recombinant protein production and characterization, of different target class proteins. As well as work in partnership with global colleagues to ensure the delivery of high-quality protein reagents to projects and contribute with novel ideas and using discernment and knowledge where appropriate to influence project progression.

You will regularly work across functional boundaries to define what is needed for discovery projects and lead protein work to deliver to that. With your knowledge in a range of procedures relating to construct design, protein expression and purification of a diverse set of target proteins, you will plan and conduct laboratory projects and experimental strategies, develop methods and technologies, generate, interpret and report scientific data autonomously.


Your profile
Essential in the role:
• PhD in biochemistry, biology or pharmacology or other a related field, or an MSc degree with significant relevant experience from pharmaceutical or biotechnology industry.
• Expertise and proven knowledge of a wide range of methods and technologies applied to the expression, purification and characterization of a diverse set of target proteins. E.g. construct design and protein engineering, bacterial expression, liquid chromatography, SDS-PAGE, mass spectrometry and biophysical techniques.

To be successful in this role you also need to enjoy collaboration and team work - and have the skill to interact and communicate efficiently across interfaces of global functions and fields in a multi-cultural settings. This goes hand in hand with your problem-solving and critical thinking skills, and strong delivery focus.

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

Ansök nu

Global Clinical Supply Chain Planner

Forskare, farmakologi
Läs mer Jun 20
At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.

Pharmaceutical Technology and Development (PT&D) is the bridge which turns brilliant science into actual medicines that help millions of people. We work across the entire value chain, designing and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.

Our global Clinical Program Supply Chain team is growing, and we are now looking for Clinical Supply Planner to join our team. Maybe you are one of them? This is a relatively new role in our organization, and you will have a fantastic opportunity to shape & develop the role to drive maximum value for the organization.


About the position
As a Clinical Supply Planner you will translate the programme level demand into a supply plan and execute the plan. This will be accomplished by developing and executing optimized plans inline with the Clinical Supply Chain Strategy. You will work closely with Clinical Supply Chain Programme Leads (CSPL) and Clinical Study Leads to match demand & supply and ultimately deliver lifechanging medicines to patients.

Responsibilities
Accountabilities include:
• Translating demand in to supply plans, which meet the inventory strategy set out by the Programme Lead (CSPL)
• Providing forecasts to our supply chain partners for each of the bill of material levels in the supply chain
• Executing the supply plan to ensure kits are available to meet patient demand
o placing orders with a range of supply chain partners
o tracking progress & escalating issues
o ensuring timely release of materials through co-ordination of supply chain team
• Owning inventory; Creating and allocating material to match individual study demand & maintaining accurate stock keeping records

Your profile
Required Skills & Knowledge
• Degree in supply chain related or drug development discipline or equivalent qualification or experience.
• In depth knowledge of R&D supply chain and drug development processes.
• Knowledge of pharmaceutical production, supply chain principles, good manufacturing practice, Food and Drug Administration requirements (or equivalent) and Customs rules and regulations.
• Proficient IT skills and an aptitude for systems.
• Excellent analytical skills and an interest in using data to drive decisions
• Super user for our key supply planning tools

Additional Requirements
• Demonstrated technical skills and mindset in supply chain management including supply planning & inventory management
• Experience of supply chain management tools
• Good understanding of the principles of risk.
• Good influencing, negotiating and problem-solving skills, including across functional, geographical and cultural boundaries.
• Demonstrated experience of training and coaching colleagues
• Excellent English written and verbal communication skills.

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

Ansök nu

Global Clinical Operations Program Director

Forskare, farmakologi
Läs mer Jun 21
The Global Clinical Operations Program Director (GPD) is a core global role within the Clinical Operations function of Late Stage R&D (Biopharmaceuticals and Oncology). The span of responsibilities is broad and may support one or several products depending on their size and complexity. The products supported will be in Phase 3 development or on the market, but the program may include studies in all phases of drug development. The GPD has a delegated, from Senior Global Clinical Operations Program Director (Sr GPD), responsibility for oversight of a program of global clinical studies, covering all clinical program deliverables to scope, quality, budget, time, resource and risk, ensuring new innovative design and delivery models are used appropriately. The role involves integrating strategy, design, feasibility and operational planning to ensure clinical drug development programs are aligned with priorities and strategy. The GPD will develop the core clinical program components for governance interactions with the oversight of the Sr GPD. The GPD acts as the lead for cross-functional teams in delivery of clinical activities assigned.
The GPD may provide project leadership for cross-functional clinical submission teams in support of regulatory marketing applications and post registration product maintenance deliverables.
Additionally, the GPD may lead or contribute to improvement and change projects within clinical operations and/or other business areas.

Responsibilities
Typical Accountabilities and Responsibilities (delegated by Sr GPD)
• Lead cross functional teams of experts in the planning and delivery of a defined clinical program of studies and/or clinical activities to scope, quality, budget, time, planning the resource and managing risk.
• Work closely with global study leaders to provide appropriate strategic oversight of a program of studies on behalf of Sr GPD and Clinical Program Team (CPT)
• Provide clinical operations expertise into the project (e.g. country selection, feasibility, operational input into design, risks and external partner management) using new innovative design and delivery models to support governance interactions and project start-up.
• Responsible for providing clinical operations expertise into the development of new business case opportunities for review by governance bodies (cost, timelines, quality, feasibility, risk)
• Lead cross functional Clinical Submission Teams in planning and execution of clinical contribution to Marketing Applications, maintenance support for regulatory interactions and reports and inspection readiness.
• Lead large or complex deliverables and the process to identify and solve or escalate operational issues. Drive delivery to plan through internal or external partners (alliance partners, Clinical Research Organizations (CROs), vendors and Academic Research Organizations (AROs)).
• On behalf of CPT, responsible for managing clinical plans (cost, FTEs and timelines) in business reporting system, such as PLANIT.
Internal Job Description
• Act as AZ point of escalation for study teams for external (e.g. CRO) partners for externally managed/outsourced studies as appropriate
• Responsible for leadership and program management of non-drug project work as assigned, e.g. cross functional improvement/change initiatives.
• Contribute to functional and cross-functional initiatives as Subject Matter Experts
• Mentor, coach and support people development as appropriate.
• Actively participate in networking both within and outside the therapeutic area, sharing best practises and lesson learnt.
• Be an early adopter for new ways of working and act as ambassadors for change, driving the implementation and utilization of new initiatives.

Your profile
Essential
• University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research. Advanced degree is preferred.
• At least 10 years’ experience from within the pharmaceutical industry or similar large multinational organization.
• Proven knowledge of project management tools and processes
• Proven experience of clinical development / drug development process in various phases of development and therapy areas.
• Proven ability to learn by working in multiple phases, TAs and/or different development situations.
• Experience from leading clinical projects and deliverables or similar expertise from other areas of drug development (such as pharmaceutical development).
• Ability to mentor, develop and educate staff

Desirable

• Project management certification
• Knowledge of process improvement methodology such as Lean Sigma/Change Management
• Regulatory submission experience
• Proven knowledge of clinical operations
• Experience with development and implementation of digital health initiatives in Clinical Studies

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

Ansök nu

Nu söker vi en Regionchef till QRIOS i Göteborg

Affärsområdeschef
Läs mer Jun 2
Drivs du av att motivera och leda andra? Är du affärsorienterad och gillar utmaningar? Är du nyfiken och låter dig inspireras av att skapa något unikt? Då kan detta vara tjänsten för dig!

På QRIOS jobbar nyfikna experter inom Life Science & Engineering. Vi är ett konsult- och rekryteringsbolag som är starkt inspirerade av de som aldrig slutar leta efter nya lösningar.


Om tjänsten
Som Regionchef kommer du ha ett övergripande ansvar för den operativa verksamheten med fokus på tillväxt, lönsamhet och att utveckla QRIOS Life Science & Engineering till ett marknadsledande bolag. I rollen förväntas du att skapa nya affärsmöjligheter samtidigt som du får möjlighet att stärka befintliga kundrelationer med ledande bolag inom Life Science & Engineering. Som Regionchef kommer du att inneha en coachande roll där du möjliggör för teamet att nå sina ambitiösa mål samtidigt som du spelar en viktig roll i deras karriärsutveckling.

Du tar över ett kompetent och energiskt team som drivs av utveckling och affärsmannaskap. QRIOS befinner sig i en expansiv fas med höga mål i sikte där vi vill bli det självklara valet när det kommer till specialistrekrytering- och konsulting inom Life Science & Engineering. Teamet består idag av 6 personer med gedigen erfarenhet av branschen. Ditt ledarskap kommer att präglas av att stötta och motivera dina medarbetare till framgång!

Dina arbetsuppgifter i huvudsak
• Resultat- och budgetansvar
• Strategisk utveckling av bolagets processer
• Affärsutveckling, försäljning och profilering av bolaget
• Personalansvar (lönesättning, kompetensutveckling, övriga personalfrågor)
• Coachning och stöttning genom bra ledarskap
• Utföra analyser av marknaden för att säkra en strategisk tillväxt
• Att kontinuerligt utveckla bolagets erbjudande mot kund

Vem är du?
För att axla denna roll bör du vara resultatdriven och ha en helhetsöverblick av affären och marknaden i stort med huvudsaklig fokus på försäljning. Du är energisk, nyfiken och trivs bäst i en händelserik miljö med stort eget ansvar och många sociala kontaktytor. Du är självgående och driver affärsenheten självständigt men samarbetar även väl tillsammans med dina medarbetare. Sälj & nätverkande är avgörande för att lyckas i tjänsten och du har ett tydligt fokus på att bygga långsiktiga och starka relationer samtidigt som du har en förmåga att agera snabbt vid behov. Vi värdesätter flexibilitet och för oss är frihet under ansvar ett vinnande koncept!

Kvalifikationer

Vi ser gärna att du har
• Akademisk examen (med fördel inom Life science och/eller Engineering)
• Erfarenhet av försäljning samt stor vana att interagera med kunder
• Tidigare budget- och resultatansvar är meriterande
• Förmåga att inspirera och motivera medarbetare och samtidigt leda verksamheten mot uppsatta mål
• Förmåga att göra affärsmässiga bedömningar av uppdrag och affärsmöjligheter samt skapa hållbara strategier för framtida verksamhet.
• Meriterande om du har erfarenhet från konsult- eller rekryteringsbranschen

Vi erbjuder
• En transparent och lyhörd kultur där dina idéer och initiativ uppmuntras och uppskattas
• En spännande tillväxtresa inom ett expansivt bolag på en het marknad
• Kunniga, trygga, nyfikna och erfarna kollegor
• Ett socialt och kompetent team där alla arbetar för våra kunders bästa och för att ha roligt och utvecklas tillsammans
• En arbetsplats där samarbete, kompetens och utveckling står högt i kurs


Om verksamheten
På QRIOS jobbar nyfikna experter inom Life Science, Engineering som vill attrahera de bästa medarbetarna, för att kunna fortsätta hjälpa våra samarbetspartners med den viktiga kompetens de efterfrågar. Vi är ett konsult- och rekryteringsföretag som är starkt inspirerade av dem som aldrig slutar leta efter nya lösningar. Som vi säger, QRIOS MINDS GO FURTHER.

Besök vår hemsida https://www.qrios.se/ eller kontakta oss direkt för att få veta mer om vilka vi är och varför just du ska söka dig till oss.

Vid eventuella frågor om tjänsten vänligen kontakta rekryteringskonsult Elizabeth Darevik, elizabeth.darevik@qrios.se

Tjänsten är på heltid med direkt anställning hos QRIOS Life Science & Engineering i Göteborg.

Urval sker löpande, ansök därför redan i dag, varmt välkommen med din ansökan!

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Drug Product Delivery Operator

Forskare, farmakologi
Läs mer Jun 1
We are curious, creative, and open to new ideas and ways of working. Above all, we are passionate about science and driven to always put patients first. Join AstraZeneca and apply your expertise in a company that are following the science and turn ideas into life changing medicines. We have an exciting opportunity for talented DPD Operators to be based in Gothenburg, Sweden.

Drug Product Delivery (DPD) within Pharmaceutical Technology & Development is the sole internal AstraZeneca department that packs, labels and distributes investigational medicinal products to clinical trial patients. We support launched, pre-launched and products under development within all our therapeutic areas. We work in a fast paced environment where flexibility and agility enable us to deliver high value to early phase clinical trials.

About the position
The DPD Operator role will be a flexible role within Drug Product Deliveries three operational skill areas, Material Management, Pack Label and Distribution. We work in a environment where flexibility and agility enable us to deliver high value to early phase clinical trials. To complement our existing team, candidates with the following experiences is of interest:

- Distribution experience from a complex supply chain organization
- Knowledge / expertise in working with automated/semi-automated equipment in an operational environment
- Drug Product Knowledge including management of Item/article and lot/batch management to ensure traceability on items/articles in a patient kit including a drug product, packaging material and patient labels from the pharmaceutical industry

Responsibilities
Main Duties and Responsibilities
The role holder will contribute to the DPD organization applying their expertise in the complex and regulated GMP environment. The work is focused on being flexible and operational within at least two skills. As a DPD operator you will perform and document all the operational work according to written procedures. Be engaged in the development and improvement of internal processes and manage deviations. Be responsible for writing of GMP and SHE procedures within own skill areas and will be responsible for related training and compliance activities. As required maintain defined facilities or equipment according to GMP standards and be proactive to contribute to projects/activities through applying specialist knowledge within appropriate areas.
Material Management & Distribution responsibilities example
Preparing documentation, receiving and packing of investigational medicinal products to clinical trials. Being the main point of contact when it comes to distribution questions for a number of studies.
Pack & Label responsibilities example
Handling batch documentation, primary pack(tablets or capsules in bottles) and secondary pack(labeling of bottles, devices and vials). Being responsible for equipment (manual and automated) including instructions, training, qualification etc.

Your profile
Essential requirements and skills
? BSc/MSc in chemistry/pharmacy/engineering or equivalent experience. Preferably 2 years experience within pharmaceutical development
? Demonstrated ability to work with teams in a culturally diverse, complex and changing environment most internally but to some extent externally
? Curious and innovative mindset with problem solving ability - resolve issues with minimal guidance
? Good written and verbal English communication and understanding

Beneficial requirements and skills
Understanding of principles, applications and management of SHE and GMP in an R&D environment
? Understanding the disciplines in Drug Product Delivery, Supply Chain and Pharmaceutical development in order to contribute to an effective Supply Chain organization

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

Ansök nu

Konsultchef till QRIOS Life Science & Engineering

HR-konsult/PA-konsult
Läs mer Jun 1
Affärsdriven konsultchef till QRIOS Life Science & Engineering


Om tjänsten
Är du en person som gillar att jobba i en flexibel miljö med växlande arbetsuppgifter och stor frihet? Vi utökar just nu vårt team med en mångfacetterad, säljande och driven konsultchef som vill vara med och utveckla vår nya och expansiva verksamhet i Göteborg!

Du ingår i vårt dotterbolag QRIOS Life Science & Engineering som är en del av Poolia-koncernen och kommer att arbeta tillsammans med rekryterare, laboratorieingenjörer, konsultchefer ja listan är lång över oss alla som samarbetar för att lyckas!

Dina arbetsuppgifter i huvudsak
I den här rollen är du relationsskapare, säljare och samtidigt spindeln i nätet för alla konsulter som dagligen hjälper våra kunder att lyckas med sin verksamhet. Arbetsuppgifterna är varierande och du ansvarar för bland annat:

• Kontakta och skapa relationer med dina framtida kunder
• Rekrytering av ny kompetens till dina kundteam
• Ansvar för hela HR-processen, allt från onboarding, arbetsmiljö och arbetsrättsfrågor, coachning och kompetensutveckling
• Arrangera sociala aktiviteter för kunder och kollegor.

Som en del av management-teamet i Göteborg är du en självklar första kontakt med många av våra framtida kunder och du tar stort ansvar för att bidra till att bearbeta marknaden och bygga upp våra kundkontakter genom tempo och specialistleverans.
Vi är en flexibel arbetsplats där den ena dagen sällan är den andra lik, vilket ställer krav på oss att vara kreativa och lösningsorienterade. Detta är ett perfekt jobb för dig som tyckte det var tråkigt att sitta hemma framför Teams under pandemin och längtar efter att få komma ut och träffa folk på riktigt igen!


Vem är du?
Det är en stor fördel om du har erfarenhet inom konsultbranschen sedan tidigare och plus i kanten om det varit inom Life Science- eller tekniksektorn. Har du utfört liknande arbetsuppgifter tidigare så är det också väldigt meriterande. Förutom detta så kommer din nyfikenhet och ditt driv vara det som avgör om du passar in i vårt Göteborgsteam.

Du behöver behärska svenska helt obehindrat och vara bekväm med att skriva och tala engelska.

Låter detta som ett utmärkt jobb för dig? Tveka inte höra av dig till mig om du har några frågor eller funderingar! Vi tillämpar löpande urval så passa på att skicka in din ansökan redan idag!

Om verksamheten
Det är en stor fördel om du har erfarenhet inom konsultbranschen sedan tidigare och plus i kanten om det varit inom Life Science- eller tekniksektorn. Har du utfört liknande arbetsuppgifter tidigare så är det också väldigt meriterande. Förutom detta så kommer din nyfikenhet och ditt driv vara det som avgör om du passar in i vårt Göteborgsteam.

Du behöver behärska svenska och engelska obehindrat både i tal och i skrift.

Låter detta som ett utmärkt jobb för dig? Tveka inte att höra av dig till mig om du har några frågor eller funderingar!

Ansök nu

Key Account Manager – AstraZeneca

Key account manager
Läs mer Jun 16
On behalf of our client AstraZeneca, QRIOS Life Science is now looking for several Key Account Managers for a consultant assignment. You will be joining AstraZenecas Primary Care team, to work with their exiting diabetes/cardio/renal and respiratory portfolio towards GP´s. Knowledge and experience within pharma industry sales is a success factor in this role but we also encourage applications from individuals with bio/medical experience outside pharma industry.

About the position
As part of AstraZeneca, the Nordic Marketing Company (Nordic) employs around 400 people across 5 countries and has offices located in Södertälje, Copenhagen, Helsinki and Oslo. By 2025 AstraZeneca Nordic aims to become a recognized leader in its core therapy areas and improve the lives of millions of people. This will be achieved by driving innovative science, preparing launches, building close collaboration and partnerships with key partners in health care systems, and developing high-performing teams.

We offer you your next career move into a stimulating and growing company that keeps patients in focus. Let us know why you are the perfect match for us and!

The roles is field based and located in Skåne, VGR, Östergötland, Uppsala/Gävle/Örebro and Stockholm with responsibility for driving the performance of products in the respective working area. Your focus will be customers in primary care

As Key Account Manager, you will join AstraZeneca’s strong CV-R-M and respiratory franchise, two of our key growth platforms. You will drive commercial interactions towards various partners. You will be accountable for your regional accounts securing sales and driving business in collaboration with both local and national cross-functional teams.


Responsibilities
• Pro-actively identifying business opportunities, communicating value propositions aligned to stakeholder needs and objectives and recommending solutions to drive and develop business
• Develop robust understanding of needs and perceptions of prescribers and other key partners
• Drive cross-functional and cross-regional collaboration to leverage AZ's account management capabilities
• Secure account and market access by driving activities with the right customers within the right accounts
• Build, develop and lead long-term external relationships
• Drive and implement our digital and omnichannel approach towards our customers.


Your profile
Essential requirements:
We need you to hold an academic degree or equivalent with healthcare or commercial background. You have validated and relevant sales experience in pharma industry or other strong bio-medical background, preferentially but not required, within disease areas; heart failure/diabetes/cardiovascular and respiratory.

• Commercial innovation - ability of developing, shaping and implementing impactful, customer focused activities to achieve long-term business goals
• Leadership - ability to coordinate, align and engage cross-functional team to drive activities and address needs of individual accounts
• Ability and readiness to travel within region and according to role needs
• Driver´s license required and own car to use during work travels

At AstraZeneca, we embrace partnership, both internally and externally. You will fit well if you are a person that creates trust and possesses credibility.

Your proven ability to understand, assimilate, and communicate scientific information will be as important for the role as will your excellent communication skills, fluent in both written and spoken English and Swedish. You are patient focused, able to see issues through the lens of a patient as well as the patient journey and relevant treatment options.


About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.



Please apply by registering your CV here on our website. Click on the "Ansök" button to the right. It is our recommendation that you register as much information as possible and that you attach a complete CV-document. Please check that your correct e-mail address is registered.

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Tekniker inom luftfart till Landvetter flygplats

Servicetekniker, elektronik
Läs mer Maj 18
Är du en ansvarstagande person med starkt teknikintresse? Vi på AVISEQ Critical Communication AB söker nu en tekniker inom luftfart till Landvetter flygplats.

Om tjänsten
I rollen som tekniker erbjuds du ett utmanande och stimulerande arbete i en spännande miljö inom vår luftfartsenhet med inriktning på flygledningssystem, kommunikations-, navigations- och surveillance system (CNS) samt terminalsystem. Du kommer att vara en viktig länk i kedjan att upprätthålla den tekniska säkerheten kring luftfarten och flygtrafiken. Vidare är du ansvarig för att säkerhetsställa att arbetet bedrivs enligt gällande kvalitets- och miljöanvisningar.

Dina arbetsuppgifter i huvudsak
Arbetet innefattar förebyggande och felavhjälpande underhåll av följande system:
• Flygledningssystem
• Navigationssystem
• Radio
• Radar
• Meteorologisk utrustning
• Kommunikationssystem
• IP Nätverk och PC-applikationer
• Publika system i terminalbyggnader

Flertalet av systemen på flygplatsen är av unik karaktär. Därför kommer du som tekniker att genomgå en grundutbildning och ett antal specifika påbyggnadskurser. Du får arbeta på ett företag som är en ledare inom sin bransch och du blir en del av ett team som består av ambitiösa och engagerade kollegor.
Det ingår resor i arbetet då vi även har utrustning utanför flygplatsen och på närliggande flygplatser. Du kommer tillhöra ett team om 10 Serviceingenjörer på Landvetter flygplats och ett större team som omfattar hela södra Sverige. Du kommer att ingå i en beredskapslista med schemalagd arbetstid.


Vem är du?
För att trivas med och lyckas i rollen som Tekniker på AVISEQ är du självständig och drivande men har samtidigt lätt för att samarbeta, både med kollegor och med våra kunder. Du har en kreativ och lösningsorienterad inställning till hur du utför ditt arbete och du har ett brinnande teknikintresse.

Vi tror att du har minst 3-årig teknisk gymnasieutbildning eller en högskoleingenjörsutbildning alternativt en motsvarande relevant arbetslivserfarenhet. Vi ser gärna att du har yrkeserfarenhet och kunskaper om radioteknik, analog/digital elektronik, mekanik samt erfarenhet av underhåll på teletekniska system. Erfarenhet av förekommande utrustning och instrument samt PC-baserade stödsystem är starkt meriterande. Du har en god kommunikativ förmåga i svenska och engelska. Du har B-körkort.


Om verksamheten
AVISEQ verkar inom kritisk kommunikation. Vi är specialister på att erbjuda kostnadseffektiva tjänster utan att göra avkall på säkerheten. Vi övervakar, driftar och underhåller våra kunders tekniska utrustning och system, allt för att säkerställa deras kritiska verksamhet. Våra största kunder verkar inom luftfart och säkerhet vid flygtrafikcentraler, flygplatser, statliga myndigheter och företag, såväl offentliga som privata, i hela Sverige. AVISEQ har cirka 200 anställda och blev i maj 2020 en del av LFV-koncernen. Vi vill vara den bästa arbetsplatsen för dig som gillar utmaningar och att ta ett samhällsansvar!

Tjänsten är en tillsvidareanställning på 100%, där vi tillämpar 6 månaders provanställning. Grund för anställning är godkänd registerkontroll/säkerhetsprövning och tillträde sker enligt överenskommelse.

Urval sker löpande, så ansök nu.

För mer information besök gärna https://aviseq.se/

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Systemadministratör till AVISEQ i Göteborg

Systemadministratör
Läs mer Maj 19
AVISEQ NMC, Network Management Center, är inne i ett intensivt utvecklingsskede och expanderar inom alla kategorier. Därför söker vi nu fler Systemadministratörer till vårt team. Vi gör nu en större satsning där vi fokuserar på att bygga upp en leveransförmåga inom området Infrastruktur innehållande datacenter, virtuella miljöer med RedHat OpenShift.

På AVISEQ arbetar vi med att bygga, utveckla och underhålla samhällskritiska system i utmanande och spännande miljöer. Du kommer in i ett härligt team där humor är lika självklart som kunskapsdelning och hjälpsamhet.


Om tjänsten
I rollen som Systemadministratör arbetar du både förvaltande i vår interna systemmiljö samt utvecklande tillsammans med våra kunder där du är med i hela processen från förstudie och analys till design, installation och drift av deras miljöer.

Dina arbetsuppgifter i huvudsak
• Arbete i kundrelaterade projekt med VMware-relaterade lösningar
• Teknisk konsultation i uppdrag mot kund, medverka vid kundmöten
• Tekniskt stöd för vår NOC (1st line – Network Operation Center)
• Utbilda kollegor vid behov
• Teknisk förvaltning av befintliga produkter

Du får arbeta på ett företag som är en ledare inom sin bransch och du blir en del av ett team som består av ambitiösa och engagerade kollegor. Som Systemadministratör får du chansen att vara med och påverka vår verksamhet och bidra till vår marknadsledande position.


Vem är du?
För att trivas med och lyckas i rollen som Systemadministratör på AVISEQ är du självständig och drivande men har samtidigt lätt för att samarbeta, både med kollegor och med våra kunder. Du är ansvarstagande och systematisk och gillar ordning och reda. Du har en kreativ och lösningsorienterad inställning till hur du utför ditt arbete och du har viljan att ständigt uppdatera dina kunskaper.

Vi ser gärna att du har minst 5 års erfarenhet av arbete med VMware (vSphere, vSAN), Linuxmiljö och Microsoft Server. Vi tror att du i botten har en högskoleutbildning med inriktning på IT. Du är flytande i svenska och engelska både i tal och skrift.
Du välkomnas till ett företag där det är högt i tak och där vi lägger stort värde i de personliga egenskaperna. Grundläggande kunskaper från RedHat (OpenShift), lagringslösningar, Active Directory, Microsoft och Scripting-erfarenhet är mycket meriterande.


Om verksamheten
AVISEQ verkar inom kritisk kommunikation. Vi är specialister på att erbjuda kostnadseffektiva tjänster utan att göra avkall på säkerheten. Vi övervakar, driftar och underhåller våra kunders tekniska utrustning och system, allt för att säkerställa deras kritiska verksamhet. Våra största kunder verkar inom luftfart och säkerhet vid flygtrafikcentraler, flygplatser, statliga myndigheter och företag, såväl offentliga som privata, i hela Sverige. AVISEQ har cirka 200 anställda och blev i maj 2020 en del av LFV-koncernen. Vi vill vara den bästa arbetsplatsen för dig som gillar utmaningar och att ta ett samhällsansvar!
Tjänsten är en tillsvidareanställning på 100%, där vi tillämpar 6 månaders provanställning. Grund för anställning är godkänd registerkontroll/säkerhetsprövning och tillträde sker enligt överenskommelse.

Urval sker löpande, så ansök nu.

För mer information besök gärna https://aviseq.se/

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Regulatory Affairs Manager, Respiratory and Immunology

Forskare, farmakologi
Läs mer Jun 7
Do you have knowledge within Regulatory Affairs and want to develop your skills within project management?

At AstraZeneca, we offer you a unique experience to work in cross functional teams with all phases of drug development, from clinical trials to marketing authorization applications worldwide. You will lead the end-to-end planning, coordination and execution of our submissions and contribute to regulatory submission strategy. Does this match your skills and ambitions for the future? Then join us to develop future treatments in the Respiratory and Immunology Therapy Area.

At AstraZeneca, we are more than 65.000 people in over 100 countries. Our aim is simply to positively impact patients’ lives together, as our pipeline of innovative medicines consistently grows. As an industry leading Regulatory function, we’re focused and committed to the development of our products as well as to our people.

About the position
We are now seeking new members to join our Regulatory Affairs Management team within the Respiratory and Immunology Therapy Area, in the role as Regulatory Affairs Manager (RAM).The role will be based at AstraZeneca’s dynamic R&D site in Gothenburg, Sweden. With employees from more than 50 countries, our Gothenburg site is a truly inspiring place to work.

Working in the role as Regulatory Affairs Manager (RAM) you will contribute to regulatory submission strategy, identify submission risks and opportunities, while leading simple through more complex regulatory applications and managing procedures through approval.

Responsibilities
Your main accountabilities/responsibilities:
• Lead and/or contribute to the planning, preparation, and delivery of submissions of varying complexity throughout the product’s life cycle from either a global and/or regional perspective.
• Provide regulatory input/ expertise on procedural and documentation requirements as defined by Health Authorities for assigned deliverable(s) including submission delivery strategy of all dossiers and all application types per market and/or region and review of documents, e.g., response documents, study protocols, periodic safety reports
• Support operational and compliance activities for assigned regulatory tasks
• Provide coaching, mentoring and knowledge sharing within the regulatory skill group
• Contribute to and lead process improvement
• Identify regulatory risks and propose mitigations to appropriate member of cross functional teams

Your profile
To be successful in this role, we believe that you have a
• University degree in science or a related field
• Minimum of 2 years of regulatory experience within the biopharmaceutical industry or similar.
• We believe that you possess good project management skills as well as leaderships skills
• Excellent written and verbal communication skills.
If you have previous experience in leading multi-disciplinary project teams, this will be an advantage.

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

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Biobank Scientist, Biosamples

Forskare, farmakologi
Läs mer Jun 7
Biobank scientists are responsible for the storage and timely supply of human biological samples (HBS) to AZ research projects. HBS are received from e.g. clinical studies or academic collaborations, stored in local biobanks and distributed to projects. The group primarily supports the Sweden Region but partners with other Biobank groups within the Biosamples department globally to provide efficient support across AZ and our partner organisations.

The Biobank group works collaboratively to provide support within agreed service levels with a strong focus on our customers. We strive hard to understand what fits their needs best and to add value through our services. With an increased focus on the value and use of biobank samples we actively seek ways to improve our process or exploit new technology to build a cutting edge facility.


About the position
We are currently recruiting for a temporary Biobank Scientist in the AZ Gothenburg Biobank group within the global Precision Medicine and Biosamples organization. This position will provide the opportunity to work in a dynamic and enthusiastic environment whilst supplying a critical service to drug discovery projects. The work is highly collaborative with the team having a collective responsibility for the overall delivery.
The role is focused on supporting drug discovery projects within R&D Gothenburg by maintaining a high quality handling and storage of HBS and support projects with requested samples in a timely manner.

Responsibilities
• Work as part of the team rotating between the following typical tasks
• Receive and register incoming HBS
• Process requests for HBS to customers
• Manage customer orders using specialized informatics systems as well as databases
• Responding to customer queries via mail or telephone
• Partner with Biobank groups globally as well as internal and external customers and stakeholders

• Act upon day-to-day issues that occur whilst processing HBS samples to ensure continuous improvement
• Identify initiatives to improve efficiency or quality.

The group has a strong emphasis on continuous improvement which takes the form of individual and group projects within the team, the department and across Biobank groups within AZ.


Your profile
Minimum experience

You should ideally have a degree in a Bioscience or Chemistry discipline and previous experience of laboratory work handling biological samples. Previous knowledge and experience of biobanking is preferred. Experience of working with various IT solutions, including extensive knowledge of Excel, LIMS systems and database usage, is also a clear advantage.
The biobank team is a highly collaborative group working to tight delivery schedules so the ability to be comfortable working at a fast pace with a goal orientated and team focussed attitude is essential. Excellent communication skills with a proactive and service minded approach is key.

Preferred experience/requirements
Experience of automated liquid handling and/or tissue sectioning is advantageous. Good analytical and problem-solving skills involving large and complex datasets

Key Attributes
• Ability to plan, perform and evaluate experiments to investigate improvement possibilities in a process
• Knowledge of the drug discovery process
• Interest in logistics and developing processes through customer interactions and technology awareness
• Drive and enthusiasm to solve the root cause of problems and not only overcome the presenting problem
• Thrive on working in a committed team and gain satisfaction from the overall performance of the group

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

Ansök nu

Scientist, Early R&I Research and Early Development, Bioscience In Vivo

Forskare, farmakologi
Läs mer Jun 7
Are you an experienced scientist ready to apply your skills in a diverse and dynamic organization? If you can envision providing scientific expertise in a role that can impact patients’ lives – join us now!
At AstraZeneca, we believe in the potential of our people and you’ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us.


About the position
We are now looking for an In Vivo Scientist with excellent laboratory skills and a drive for innovation to join the Bioscience in vivo department within the Early Respiratory and Immunology (eR&I) R&D unit located in Gothenburg, Sweden.
Respiratory and immunology are two of AstraZeneca’s main therapy areas. From a research perspective we work to understand, treat, modify and ultimately cure respiratory disease with an emphasis on four respiratory diseases with significant unmet medical need; asthma, COPD, Idiopathic Pulmonary Fibrosis (IPF) and Chronic Cough. In addition, we also focus on immunology-driven disease areas including rheumatology, dermatology, gastrointestinal and inflammatory diseases driven by eosinophilic immune dysfunction.
The successful candidate will join a highly motivated team that works closely together with other departments focusing on target identification, drug formulation, translational science, in vitro assay development and drug metabolism/pharmacokinetics to support discovery projects and to drive new exciting research. Are you ready to join us?

Responsibilities
As a vital member of the in vivo team you will contribute to progress our drug discovery projects. Your role will be mainly lab-based in which you will be actively involved and responsible to coordinate and perform in vivo experiments. While we expect you to be independent we are also looking for someone that thrives in a team setting and contributes to the success of others.

Your profile
• B.Sc. or M.Sc. degree in relevant subjects or equivalent level of understanding developed through experience in drug discovery or early development
• Excellent technical and experimental In vivo experience and skills, including rodent handling, drug administration and collection of biological samples. Ability to coordinate and perform respiratory disease and mechanistic models.
• Valid certificates to work with live animals in Sweden
? Be respectful, communicate openly and show effective collaborative behavior to obtain high quality study results
? Excellent written and oral communication skills in English.
? Excellent organization skills
? Ability to incorporate the views of others in your communication
? Maintain the highest standards of animal welfare and ethical compliance and ensure integrity of generated data. Familiar with using Good Statistical Practice in animal research and applying the 3R’s (reduction, refinement and replacement) across the full range of studies
? Good generic computer proficiency including Microsoft Office.

Desirable for the role
? Experience in basic cellular and molecular biology techniques (e.g. ELISA,western blot, FACS, Meso Scale Discovery (MSD) technology platform), and RNA (qRT-PCR, RNASeq)
? Ability to interpret and analyze generated data
? Good written and oral communication skills in Swedish and experience in writing ethical applications for animal work in Sweden
? Good understanding of pharmacology, physiology, immunology, respiratory diseases (COPD, asthma, cough, IPF) and PKPD relationships


About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg until 2022-12-23 with possibility of extension. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

Ansök nu

Analytical Scientist

Forskare, farmakologi
Läs mer Maj 23
About the position
Do you have an interest in analytical chemist? Would you like to work in a cross-functional environment using state of the art technology? Then you might be our next member in the Separation Science Laboratory team!

We’re looking for a talented and motivated analytical chemist to join our Separation Science Laboratory team within the Pharmaceutical Science function at AstraZeneca in Gothenburg.
The vision for Pharmaceutical Sciences is to deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes and manufacturing of Active Pharmaceutical Ingredients (API). Our portfolio of projects spans traditional small molecules to nucleotide-based therapies and nanomedicines across AstraZeneca’s therapy areas.

Responsibilities
You will join a highly competent team and collaboratively drive the delivery of pure compounds to our early portfolio. We use modern chromatographic instrumentation including LC and SFC in both analytical and preparative scale and a high degree of automation.
To be successful in this role you will need a problem-solving attitude and strong delivery focus. It is essential with good communication skills and ability to engage and collaborate across boundaries. You are expected to:

• Be laboratory based and work collaboratively with colleagues
• Run chromatographic equipment as well as liquid handling robotics
• Effectively operate with scientists from other functions in a highly cross-disciplinary environment

Your profile
Essential requirements
• Scientific knowledge within analytical chemistry
• Technical skills and experience to use and maintain chromatographic equipment
• Excellent problem-solving skills
• Excellent English, both spoken and written
• Work collaboratively, prioritise your own work and act decisively

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

Ansök nu

Senior Scientist, In Vivo Cardiovascular Biology

Forskare, farmakologi
Läs mer Maj 23
About the position
Senior Scientist, In Vivo Cardiovascular Biology, is a lab based role where you will explore novel drug targets and support existing projects with key in vivo and ex vivo data. Collaboration is critical for successful delivery of drug projects and you will work closely with scientists/teams from a wide range of different functions within AstraZeneca as well as with external partners and collaborators. Your in vivo work will include experimental work in small animals to broaden the pharmacodynamic and pharmacokinetic understanding of our new drug candidates as well as cardiovascular disease. You will have the opportunity to explore novel techniques and ideas required for progressing existing portfolio and novel science. Some in vitro work can also be part of the role description.

Responsibilities
• Independently design, develop, and run experiments as well as analyse results, interpret data and report in vivo studies and ex vivo assays for projects from pre-target identification to clinical stage
• Communicate data and scientific findings at internal and external meetings and through publications in scientific journals
• Proactively contribute to a vibrant and innovative working environment where improvements and new ideas are adopted and freely shared

Your profile
Essential for the role
• Master or PhD in biology, pharmacology, cardiovascular biology or similar
• Hands-on experience and expertise in handling mice and rats and performing in vivo experiments accordingly
• Entrepreneurial, collaborative and flexible ways of working
• Strong oral and written communication skills
• Excellent English, both spoken and in writing

Desirable for the role
• Scientific background in any of the following fields: cardiovascular disease, heart failure, cardiac regenerative medicine, cardiac metabolism, genetic cardiomyopathies
• Experience with performing open chest surgeries , such as myocardial infarction and intramyocardial injections
• Knowledge and experience in ultrasound imaging and/or MRI imaging
• Background in drug discovery and development in the pharmaceutical industry

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

Ansök nu

Formulation/Analytical Scientist

Forskare, farmakologi
Läs mer Maj 24
Do you enjoy working in the lab and have experience within formulation and analytical characterization of active pharmaceutical ingredients? Are you interested in developing liquid formulations for early in vivo studies? Do you enjoy to work collaboratively with and learn from highly motivated and skilled scientists? We are looking for you that are a formulation and analytical chemist with experience in the pre-clinical phase of drug development.

AstraZeneca is now seeking a Formulation/Analytical Scientist to join our Small Molecule Preformulation and Biopharmaceutical team within the Advanced Drug Delivery (ADD) function that is part of Pharmaceutical Sciences at AstraZeneca in Gothenburg, Sweden.

At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big, and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re the one we are looking for. Pharmaceutical Sciences at AstraZeneca delivers the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) and drug products. Our portfolio of projects spans traditional small molecules, peptides, oligonucleotides to RNA based therapeutics across AstraZeneca’s therapy areas. Advanced Drug Delivery (ADD) resides within Pharmaceutical Sciences with a mission to provide novel products to AstraZeneca’s clinical pipeline.

About the position
As a Scientist working in the pre-clinical development phase within ADD you will support drug projects from a formulation perspective, from the first in vivo studies to candidate drug nomination. You will focus on various small molecule projects and develop formulations and analytical assessments for PK, PK/PD studies, and toxicology studies. You will work as a member of pharmaceutical project teams, and in close collaboration with other analysts, formulators, solid state, biopharmaceutics experts at AstraZeneca.

Preferably, you should are experienced in formulation chemistry as well as in analytical chemistry and have previously been exposed to an industrial setting. You should possess an enthusiasm for laboratory-based work, be flexible and have a collaborative and problem-solving mind-set. We are looking for a scientist with good communication and planning skills, balanced with the ability to work independently. In addition, you will need a strong sense of responsibility, team work and delivery focus.


Responsibilities
• Support drug development projects with formulations for pre-clinical in vivo investigations.
• Perform essential characterization of the formulations e.g. content, impurity, pH and particle size measurements to support studies like stability, homogeneity etc.
• Generate, evaluate and report data clearly and reliably in accordance with current standard procedures.
• Give formulation/analytical support to scientific initiatives together with other specialists within these areas.
• Working as a member of cross-skilled drug development project teams.

Your profile
Essential Requirements

• MSc degree in a scientific discipline relevant to formulation/analytical science (e.g., chemistry, pharmaceutical technology, surface & colloid chemistry or equivalent qualifications).
• Basic knowledge of analytical methodologies such as spectrometry, separation science (U/HPLC) and physical particle characterization, i.e. particle size measurements.
• Understanding of principles and applications of Good Laboratory Practices (GMP/GLP).
• Ability to communicate in English both orally and in writing.

Desirable Requirements

• 3+ years of industrial experience of formulation work focused on small molecules in pre-clinical drug development phase.
• Profound knowledge within liquid based formulation science as well as analytical chemistry.

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

Ansök nu

Lead Project Engineer

Civilingenjör, kemiteknik
Läs mer Maj 16
Are you a Senior Chemical or Mechanical Engineer with great experience from the Process industry? Do you like to work interdisciplinary, utilizing your knowledge and experience in different projects? Then this might be the optimal position for you!

Valmet is now looking for a Lead Process Engineer to join the Gothenburg organization.

Valmet is a leading global developer and supplier of process technologies, automation and services for the pulp, paper and energy industries. The company has over 220 years of industrial history and a strong track record in continuous improvement and renewal.

Valmet is organized around five business lines and five geographical areas. The business lines are Services, Pulp and Energy, Paper, Automation Systems and Flow Control. The areas are North America, South America, EMEA (Europe, Middle-East and Africa), Asia Pacific, and China. The areas are responsible for sales, providing services that meet customers’ needs and support of project deliveries in their respective regions.

Responsibilities
• Design and lead process work .
• Work with Sales projects, Customer order projects as well as R&D projects.
• In Customer order projects you will participate in commissioning, start-up, test run and inspections of the plants.
• Participate in negotiations.
• Participate in the Continuous Improvement activities
• Process oriented, support continuous improvements and efficiencies within the team.


Your profile
To be successful in this position we expect you to have:

• An engineering degree or similar.
• At least 10 years of experience from working in the industry.
• Pressure vessel design experience.
• An innovative mind with a problem-solving focus.
• Broad skills in technical calculations, AutoCAD and Solid Works.




About the organisation
This is an consultant assignment at Valmet for six months with possibility of extension. During this time you will be hired by QRIOS.

QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you. Being a consultant at QRIOS gives you opportunities to try different industries, companies and roles.

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Junior CAD Engineer for Pressure parts & Plant Engineering

Processingenjör, maskin
Läs mer Maj 16
About the position
Valmets Pressure parts & Plant department is looking for a junior Cad Engineer to join our highly skilled team. We deliver service projects for the pulp and energy business. Our projects are global and in all sizes from shorter, day long projects to several months.

We work as a team and your task will be to be the design engineer supporting a lead engineer.
Our goal is to find someone to grow into the company and in the long-term wanting to continue their career at Valmet.


Responsibilities
• Manufacturing and installation drawings
• Weld lists
• Necessary calculations
• Together with the responsible lead engineer, follow the project development and time schedules.


Your profile

• Technical Education, preferably a B.Sc in mechanical engineering or KY education
• Autocad
• E3D
• Solidwork





About the organisation
This is an consultant assignment at Valmet for six months with possibility of extension. During this time you will be hired by QRIOS.

QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you. Being a consultant at QRIOS gives you opportunities to try different industries, companies and roles.

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Senior Research Scientist

Forskare, farmakologi
Läs mer Maj 16
Senior Research Scientist – In vitro cardiac disease modelling

Are you an experienced scientist in the field of stem cells and gene editing? Would you like to contribute to the development of novel therapies?

This might be the next challenge for you!

At AstraZeneca in Gothenburg, Sweden we have an exciting opportunity for you to join us in Applied Stem Cell Sciences group in Translational Genomics, Discovery Sciences, Biopharmaceuticals R&D, as a bench-based Senior Research Scientist to be a key player in developing therapeutics to change patients’ lives.


About the position
You will be based in Gothenburg Sweden, working alongside our stem cell scientists, disease area specialists and genome editing group. Using your strong knowledge and experience in stem cell biology, cell model development and CRISPR technology you will have the opportunity to work on in vitro aspects of therapeutic genome editing projects. This includes culture, genome-engineering and differentiation of induced pluripotent stem cells (iPSCs) and genetic and functional validation of engineered lines.

The role is focused on laboratory-based activities. Your biggest impact will be through significant contributions to the practical delivery to projects in compliance with AstraZeneca corporate responsibility, policies and relevant safety standards.

It is essential to have good social and communication skills, be collaborative and a strong team player. Candidates should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude.

Good organizational, data management and documentation skills are required, and you should be comfortable in presenting your results. English language is required, both spoken and in writing.

Responsibilities
Key Responsibilities:
• Culture and differentiation of human iPSC lines to cardiac and skeletal muscle
• Perform molecular biology, biochemical, and cellular assays to evaluate the outcomes of gene editing experiments on genomic DNA, mRNA, protein, and functional levels.
• Culture of human primary cells and various mammalian cell lines.
• Effectively collaborate within a matrixed research team to facilitate the success of projects.
• Maintain complete experimental records.

Your profile
Minimum Requirements:
•PhD in Developmental Biology, Cell Biology, Gene Editing or a BSc/MSc degree with significant experience
•Proven experience with PSC biology and directed-differentiation to cardiac and/or skeletal muscle
• Demonstrable experience with cell line engineering using CRISPR/CAS9
•Design, develop, and optimize in vitro transfection/transduction experiments using a variety of perturbagens, including lentivirus/AAV-mediated infection
•Hands-on experience with the following assay platforms: RT-qPCR, ddPCR, Flow Cytometry, ELISA, Western blots, and cellular functional assays
•Experience with the culture of multiple mammalian cell types including primary cells
•Excellent communication skills with ability to build open and collaborative relationships and work effectively as a member of a multidisciplinary team
•Excellent organizational skills and documentation practices

The following skills are highly desirable:
• Experience with NGS library prep, bioinformatic analysis, and cutting-edge molecular biology methods
• Expertise with liquid handling automation technologies
• Experience of setting up cell based pharmacological assays

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.

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Tekniker inom luftfart till Landvetter flygplats

Servicetekniker, elektronik
Läs mer Apr 27
Är du en ansvarstagande person med starkt teknikintresse? Vi på AVISEQ Critical Communication AB söker nu en tekniker inom luftfart till Landvetter flygplats.

Om tjänsten
I rollen som tekniker erbjuds du ett utmanande och stimulerande arbete i en spännande miljö inom vår luftfartsenhet med inriktning på flygledningssystem, kommunikations-, navigations- och surveillance system (CNS) samt terminalsystem. Du kommer att vara en viktig länk i kedjan att upprätthålla den tekniska säkerheten kring luftfarten och flygtrafiken. Vidare är du ansvarig för att säkerhetsställa att arbetet bedrivs enligt gällande kvalitets- och miljöanvisningar.

Dina arbetsuppgifter i huvudsak
Arbetet innefattar förebyggande och felavhjälpande underhåll av följande system:
• Flygledningssystem
• Navigationssystem
• Radio
• Radar
• Meteorologisk utrustning
• Kommunikationssystem
• IP Nätverk och PC-applikationer
• Publika system i terminalbyggnader

Flertalet av systemen på flygplatsen är av unik karaktär. Därför kommer du som tekniker att genomgå en grundutbildning och ett antal specifika påbyggnadskurser. Du får arbeta på ett företag som är en ledare inom sin bransch och du blir en del av ett team som består av ambitiösa och engagerade kollegor.
Det ingår resor i arbetet då vi även har utrustning utanför flygplatsen och på närliggande flygplatser. Du kommer tillhöra ett team om 10 Serviceingenjörer på Landvetter flygplats och ett större team som omfattar hela södra Sverige. Du kommer att ingå i en beredskapslista med schemalagd arbetstid.


Vem är du?
För att trivas med och lyckas i rollen som Tekniker på AVISEQ är du självständig och drivande men har samtidigt lätt för att samarbeta, både med kollegor och med våra kunder. Du har en kreativ och lösningsorienterad inställning till hur du utför ditt arbete och du har ett brinnande teknikintresse.

Vi tror att du har minst 3-årig teknisk gymnasieutbildning eller en högskoleingenjörsutbildning alternativt en motsvarande relevant arbetslivserfarenhet. Vi ser gärna att du har yrkeserfarenhet och kunskaper om radioteknik, analog/digital elektronik, mekanik samt erfarenhet av underhåll på teletekniska system. Erfarenhet av förekommande utrustning och instrument samt PC-baserade stödsystem är starkt meriterande. Du har en god kommunikativ förmåga i svenska och engelska. Du har B-körkort.


Om verksamheten
AVISEQ verkar inom kritisk kommunikation. Vi är specialister på att erbjuda kostnadseffektiva tjänster utan att göra avkall på säkerheten. Vi övervakar, driftar och underhåller våra kunders tekniska utrustning och system, allt för att säkerställa deras kritiska verksamhet. Våra största kunder verkar inom luftfart och säkerhet vid flygtrafikcentraler, flygplatser, statliga myndigheter och företag, såväl offentliga som privata, i hela Sverige. AVISEQ har cirka 200 anställda och blev i maj 2020 en del av LFV-koncernen. Vi vill vara den bästa arbetsplatsen för dig som gillar utmaningar och att ta ett samhällsansvar!

Tjänsten är en tillsvidareanställning på 100%, där vi tillämpar 6 månaders provanställning. Grund för anställning är godkänd registerkontroll/säkerhetsprövning och tillträde sker enligt överenskommelse.

Urval sker löpande, så ansök nu.

För mer information besök gärna https://aviseq.se/

#LI-HG1

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Pharmacoepidemiologist

Forskare, farmakologi
Läs mer Maj 9
Do you have expertise in, and passion for drug safety and real world evidence (RWE)? Would you like to apply your expertise to evaluate the safety of medicines in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you! At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.

Why AstraZeneca?

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering cutting edge methods and bringing unexpected teams together. Interested? Come and join our journey. Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you.

Responsibilities
The Pharmacoepidemiologist / Senior Pharmacoepidemiologist works independently in the design, execution, analysis, interpretation, and internal and external communication of specific epidemiological studies and literature reviews. This role requires taking a leadership role in a range of activities, including delivery of experienced epidemiology strategy, support, and scientific leadership to project teams and the epidemiology global skills group, at all stages of pharmaceutical development.

They will manage externally commissioned research projects, which includes establishing, maintaining, and expanding relationships to partner effectively with external experts and research groups to negotiate time frames, provide recommendations on resource requirements, and ensure delivery of the tasks as agreed. They will promote good epidemiological practice and represents the company’s position when interacting with external experts, collaborative groups, and contract research organizations; and will keep abreast of epidemiological developments within academia, regulatory, and among key opinion leaders.

Your profile
Essential Requirements
• MSc. or Ph.D. or equivalent in pharmacoepidemiology, epidemiology or related health science field and substantial experience in the health care environment.
• Hands-on experience in utilizing secondary data and primary data collection studies and knowledge of patient safety databases for use in generating RWE.
• Ability to apply advanced epidemiological theory and techniques
• Able to provide critical appraisal to study designs and published studies
• Ability to work effectively with internal & external experts, collaborative groups and contract research organizations (CROs)


Desirable Requirements

• A broad global pharmacovigilance knowledge including knowledge of PASS studies, post-marketing commitments and reporting requirements
• Understanding of drug safety and medical terminology and ability to summarize medical information drug safety experience in a clinical or post-marketing environment.
• Ability to effectively represent epidemiology and pharmacovigilance operations on multidisciplinary teams
• Good therapeutic and disease area knowledge and knowledge of drug development and life cycle management
• Knowledge and experience with drug safety reporting and regulatory compliance and experience with international drug safety reporting/regulations, including PASS and RWE studies, Risk Management Plans and Signal Management
• Previous experience in managing communication with EMA and FDA
• Substantial knowledge and experience in epidemiological methods and research in drug development or in a closely related academic research area
• Knowledge of clinical trial activities and reporting requirements
• Experience managing complex medical evidence programmes, including studies such as pragmatic trials or/and PASS

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg or remote for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we are opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Interested? Come and join our journey.

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Research Scientist – Molecular and Cell Biology

Forskare, farmakologi
Läs mer Maj 9
Do you have a background in biochemistry or cell biology, aren’t afraid of trying new paths and doing things differently? Do you also feel passionate about the possibilities of science to change lives? Perfect, your next challenge might be this role at AstraZeneca!

A position has arisen for a highly motivated (Senior) Research Scientist – Molecular and Cell Biology to join the Cell and Molecular Pharmacology (CMP) team within the Early Cardiovascular, Renal and Metabolic (CVRM) disease area in Gothenburg, Sweden. Early CVRM is one of three main therapeutic research areas within AstraZeneca that deliver candidate drugs into late-stage clinical development. The CMP team delivers key data based on histology, imaging, biomarker, FACS and bioassay automation to support projects across the Cardiovascular, Renal and Metabolism disease areas.


About the position
The role is lab-based, providing dedicated experimental support to our drug discovery programs. The successful candidate will deliver high-quality molecular biology data to build a detailed understanding of pharmacological response and mode of action for small molecules, PROTACs and ASOs. The work includes independent planning and execution of experiments, troubleshooting and timely reporting/presentation of data according to agreed timelines.

Your profile
Essential Requirements:
• BSc/MSc degree in Molecular Biology, Biomedical, Pharmacology, Biochemistry or a related discipline with significant practical experience.
• Extensive experience in molecular and cellular biology techniques including protein and gene expression analysis, Western Blot, qPCR and cell culture. Ideally applied to relevant cellular assays and in vivo samples.
• Excellent communication skills and an ability to operate in a multi-disciplinary research environment.
• Independent analysis and evaluation of complex data and delivery of data to agreed timelines.

Desirable Experiences and Abilities:
• Experience within Cardiovascular, Renal and/or Metabolic disease areas.
• Expertise in the design, development and validation of assays for compound profiling.
• Experience in flow cytometry.
• Experience working with PROTACs and/or antisense oligonucleotides (ASOs) in Mode of Action studies and pharmacological profiling.
• Proven ability in providing technical leadership and guidance to others.
• Scientific visibility and leadership through project contributions and scientific publications.

The successful candidate demonstrates a passion for driving scientific questions through experimental work, combined with strong team working ethics. You have good social and communication skills, is collaborative and a great team player. You should also be able to work independently and have a positive, goal oriented and problem-solving attitude. Excellent English is required, both spoken and written, and good organizational skills are of use.

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we are opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Interested? Come and join our journey.

Ansök nu

Scientist – Early Product Development and Manufacturing

Forskare, farmakologi
Läs mer Maj 9
At AstraZeneca, we unlock the power of What Science Can Do. Empowered to explore, every day we work towards our ultimate aim - treating, preventing, modifying and even curing complex diseases. Be part of the team where you are empowered to follow the science!

The arena
Pharmaceutical Sciences (PharmSci) is accountable for the design and development of synthetic routes, preclinical and phase I/II formulations, encompassing both small molecules and new modalities such as mRNA and oligonucleotides, across the whole range of AstraZeneca’s therapeutic areas.

Within Early Product Development and Manufacture (EPDM) in Gothenburg, Sweden, the manufacturing teams are accountable for delivery of clinical trial material for a vast project portfolio. We have a wide range of manufacturing assets in three separate facilities, supplying different types of products and dosage forms to studies across the globe.

About the position
Within the EPDM manufacturing teams, in the GMP (Good Manufacturing Practice) arena, you will make an important contribution in delivering clinical results in the development of new medicines. This role revolves around the manufacturing of drug product where all activities below will have a significant impact on the speed, quality and cost of the AZ development portfolio.


Responsibilities
• Assume responsibilities toward timely manufacture of various drug products in line with the plans agreed within EPDM and surrounding stakeholders.
• Work with practical hands-on processes in our GMP facilities following manufacturing batch records and perform transactions in material management systems.
• Rapidly develop strong competence within relevant process technologies and build credibility and ability to work independently with a high degree of autonomy.
• Support documentation activities, e.g. by authoring manufacturing batch records, taking part in deviation investigations, authoring SOPs, and other guidance documents, change control processes etc.
• Monitor, secure and follow up on other regulatory requirements according to GMP through associated IT-systems.
• Assess records and report manufacturing and validation data accurately according to GMP.
• Ensure that SHE (Safety, Health and Environment) and GMP standards are upheld and ensure AZ Policies and Standards are understood and followed.
• Be entrepreneurial and drive initiatives to further improve flexibility and productivity, resulting in shorter lead times or increased value for our customers and patients.

In joining the EPDM and PharmSci, you will be part of an amazing group of skilled and driven colleagues who truly embrace team spirit, who you will exchange knowledge and collaborate with on many levels in various contexts. This provides excellent opportunities for your professional development, and possibilities to take on further accountabilities in line with your personal growth.

Your profile
Experience/requirements
MSc in pharmacy/engineering and/or extensive GMP-manufacturing experience from the pharmaceutical industry is essential for this role. Hands on experience with pharmaceutical manufacturing equipment, automation, complex production lines (e.g. continuous) are merits.

We are looking for a Scientist with excellent collaboration, communication, and planning skills with a strong sense of responsibility, team work and delivery focus.

Strong verbal and documentation skills in English is a requirement. We expect you to have a keen interest to learn and operate both simple and complex manufacturing equipment and develop your expertise in pharmaceutical process technology.

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for 6 months, with a possibility of extension. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development

Ansök nu

Senior Scientist Pharmacology

Forskare, farmakologi
Läs mer Maj 9
Are you an experienced Scientist ready to apply your skills in a diverse and dynamic company? If your passion is science and you want to be part of a team that makes a bigger impact on patients’ lives, then there’s no better place to be.

At AstraZeneca, we believe in the potential of our people and make the most of your skills and passion. Respiratory & Immunology is one of AstraZeneca’s main therapy areas. From a research perspective we work to understand, treat, modify and ultimately cure respiratory and autoimmune diseases such as asthma, COPD, IPF, IBD, RA and SLE.

We are looking to onboard an experienced histologist with background in image analysis and ideally some pathological assessment. A successful applicant would need to have a drive for innovation and idea generation as well as excellent laboratory skills to join the Bioscience In Vivo Department within the Early Respiratory and Immunology R&D unit located in Gothenburg, Sweden.

The successful candidate will join a highly motivated team that works closely together with other departments focusing on Target Translational Science, Bioscience In vitro assays and Drug Metabolism/Pharmacokinetics to support discovery projects and to drive new exciting research. Are you ready to join us?

About the position
What you’ll do

Contribute as a vital member of the department and in various working teams to progress our respiratory and immunological drug discovery projects. You will actively take part in scientific discussions, gain input from others and be involved in multiple project meetings to present and discuss experimental plans and data.

This is a partly lab-based role where you will be actively involved in experimental phase of histological analyses, with responsibility to coordinate, perform and evaluate experiments as well as drive the establishment of new techniques. Characterization and validation of target expression and subsequent evaluation of engagement of the target by drug treatment in both patient and in vivo tissue samples will be the key areas of your daily work. You will independently assess and report data with a clear understanding of its reliability, interpretation of findings and draw appropriate conclusions with input from others.

We are looking for a team player with strong background in histology and related image analysis techniques, ideally complemented by some experience in pathology and preclinical drug discovery processes.

Responsibilities
Essential for the role

PhD in a relevant discipline (area of Bioscience) ideally complemented by experience of working in a drug discovery environment or molecular pathology laboratory

Strong experimental histology skills in performing immunohistochemistry, histochemistry and in situ hybridization (RNAscope)

Knowledge in histology scoring and histomorphometry

Proven knowledge and experience in image analysis using commercial software solutions

To conduct where appropriate in parallel more than one area of work to agreed timelines

Be respectful, communicate openly and show effective collaborative behavior to obtain high quality study results

Excellent written and oral communication skills, including presentation skills. You are organized and incorporate the views of others in your communication and collaboration

Desirable for the role

Respiratory and immunology disease knowledge, including target and mechanism knowledge and basic understanding of?pharmacokinetics

Some experience in pathology

Understanding and experience with molecular biology

Independent experimental design, including understanding of statistical methods, quality control and data reporting/archiving

Good understanding of pharmacology, physiology and immunology


About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg until December 21th 2022, with a possibility of extension. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?

At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development

Ansök nu

Business Operations Manager till Pretzel Therapeutics

Ekonomiassistent
Läs mer Apr 25
Är du en organiserad och strukturerad person som gillar problemlösning? Har du kombinerat med detta även en bakgrund inom ekonomi eller administration? Vi söker nu en Business Operations Manager till Pretzel Therapeutics i Göteborg, ett spännande och nytänkande bolag som utvecklar banbrytande läkemedel.

Pretzel Therapeutics är ett väletablerat bolag med globala investerare som alla har en gemensam målbild - att utveckla banbrytande terapier för att hantera sjukdomar orsakade av mitokondriell dysfunktion. Man går nu in i en expansionsfas som börjar med att bygga en organisation i Sverige. För att stödja den dagliga verksamheten rekryterar vi nu en Business Operations Manager som kommer att spela en nyckelroll på Pretzel Therapeutics Sweden AB, genom att stötta FoU-organisationen i Göteborg. Detta är en rekrytering för en fast tjänst på bolaget, med stora möjligheter till utveckling inom en organisation som just nu befinner sig i expansionsfas.

Kandidater intervjuas löpande. Se till att skicka in din ansökan redan idag!

Dina arbetsuppgifter i huvudsak
Som Business Operations Manager kommer du ansvara för den dagliga operativa verksamheten inom bolaget. Du kommer jobba i nära samarbete med det amerikanska teamet för att skapa en organisation i linje med bolagets målsättning och vision. I rollen som Business Operations Manager kommer du bland annat att:

• Leda lokala affärsrelaterade aktiviteter och rapportera till Global Head of Operations i USA.
• Proaktivt identifiera nödvändiga förändringsarbeten och implementera lösningar.
• Identifiera och föreslå leverantörer för verksamheten, samt hantera kontrakt- och avtalsfrågor.
• Hantera finansiell rapportering inklusive leverantörsreskontra, löner, inköpsordrar, inventering, etc.
• Leda det administrativa arbetet för att utveckla kontors- och laboratorieverksamheten.
• Ansvara för kontorsutrustning; IT-system, servrar, printers, telefoner, datorer etc.
• Vara den primära dagliga kontaktpunkten för alla lokala samarbeten med leverantörer och partners.
• Delta i affärsrelaterade möten med kollegor i USA för att tillsammans bygga verksamheten.

I rollen som Business Operations Manager förväntas du jobba i nära samarbete med kollegor i USA, vilket innebär att du kan behöva delta i affärsrelaterade möten där din arbetstid ibland kan bli förskjuten för att matcha dina USA-baserade kollegors tidszon. Det kan även förekomma inrikes- och utrikesresor i tjänsten.

Vem är du?
För att lyckas i rollen som Business Operations Manager ser vi helst att du har:

• En högskoleexamen inom ekonomi, finans eller administration, alternativt motsvarande arbetslivserfarenhet från industrin.
• Vana att arbeta med Microsoft Office (t.ex. Excel, Word och PowerPoint) samt Zoom, MS Teams.
• Goda kvantitativa färdigheter, förmåga att skapa och upprätthålla enkla ekonomirapporter i MS Excel.
• Förmåga att snabbt lära dig nya färdigheter, lösa problem och prioriteringar bland arbetsuppgifter i en ny verksamhet under utveckling.
• Förmåga att utveckla och upprätthålla tvärfunktionella relationer.
• Förmåga att proaktivt lösa problem och fatta snabba beslut självständigt
• Mycket samarbetsvilligt och serviceinriktat tankesätt, både internt och externt.
• God kommunikationsförmåga i tal och skrift på både engelska och svenska.
• Arbetslivserfarenhet från ett bioteknik- eller läkemedelsföretag är meriterande men inte ett krav.

Om verksamheten
Pretzel Therapeutics är ett Boston-baserat bolag som under de senaste åren har startat upp verksamhet även i Göteborg. Målsättningen för bolaget är att utvecklar förstklassiga terapier som kan hantera mitokondriell dysfunktion vid dess rötter. Bolaget grundades av några av världens främsta akademiker inom mitokondriell biologi, och leds idag av duktiga experter inom läkemedelsutveckling.

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Team Manager - Automotive

Teamledare
Läs mer Apr 29
Do you have high energy and passion for leadership, recruitment, and sales, along with development of strategies and a genuine interest for engineering technologies? Are you the future leader we are looking for, to lead our Interior & Exterior team within Business Unit Engineering?

As a Team Manager you will be part of a global organization where you will have the entire Profit and Loss responsibility for the Interior and Exterior team. Our goal is to continue developing our leading position, where we help our customers to transform their products and services by co-creating point solutions, platforms & systems. Our core values Ambition & Care influence everything that we do, and we will always put our employees first.

About the position
In this role, you will lead a fast-growing team and make sure that we offer our key clients the best solutions and competence. As a Team Manager you have the full responsibility for your team, including Profit & Loss, and for the operations with your resources. You are also deeply motivated by engaging your employees, making sure that their competence gets the best possible development.

You have a genuine interest in automotive industry, with knowledge in Engineering, Function/Platform Development Processes or similar. You will create customer solutions to develop our in-house projects, which we deliver to our customers within the domain. You will be responsible for building your own team-specific competence and for allocating resources, while developing your team and environment.

Sales & Customer Relations are key components, and should enjoy the daily discussions with new and existing customers. You also ensure profitability and growth of your team through recruiting – and keeping – the right employees.

Responsibilities
As a Team Manager at Capgemini Engineering, you are the heart and soul of our company. You know what to deliver, regardless whether it is a local or global project or service.

Furthermore the role involves but are not limited to:

• Ensure the profitability of your team, while managing your employees
• Staffs your employees on best projects & assignments
• Drive and set your sales strategy and build customer relations
• Take responsibility of creating and meet agreed budget
• Collaborate with our Talent team, to recruit the right talents
• Follow the company and unit strategy
• Anticipate contract ends and resources reallocation
• Manage and support career development for your team
• Contribute to R&D projects / offers development
• Ensure renewals and upsell on your territory
• Work on technical client proposals

Your profile
In order to be successful in the role weexpect you to have the following background:

Experience
• Background from Mechanical Engineering within Automotive
• Experience from sales (preferably B2B)
• Experience preferably as a Team Manager or other leading roles (Project Manager, Product Owner, Scrum Master or similar)
• Experience from consulting business
• Fluent in English and Swedish

Personal qualities
• Quick-footed and flexible
• Structured and methodical
• People's person and service oriented
• Result-oriented person who loves to drive and execute strategy

It is a merit to have experience from project leadership and working in an international context.

Do you see yourself as a structured person with the heart in the right place. Prestige has no room at Capgemini Engineering. You are ambitious and you always strive to do “bigger and better” – a fearless go-getter with an easy going personality, and close to laughter.

Is this you? Perfect, we´re looking forward to meeting you!

We are interviewing candidates on a continuous basis and welcome your application today.


About the organisation
QRIOS Life Science & Engineering can offer several opportunities for skilled people with a background in engineering or science. We work with Sweden’s leading pharmaceutical and life science and engineering companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

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Senior Scientist in Cell Banking

Forskare, farmakologi
Läs mer Maj 4
We now have an exciting opportunity for you to join our Cell Bank SE team in Gothenburg for 1 year as a Senior Scientist. The Cell Bank, part of Discovery Sciences, is a research unit key to the functioning of a large part of Discovery R&D, through storage and supply of stocks of all mammalian cell lines used within AstraZeneca (AZ). The unit works closely with a range of customers across many AZ sites, through the purchasing of all new cell lines, provision of cell lines in culture, generation of cell banks, cryopreservation, storage, and revival of banks, as well as supply of cells to local requestors, and shipments to other sites. To be successful in the role, we see you as a person that enjoys collaboration and team work, and effective interaction across functions, disciplines, and cultures.

About the position
This role will be focused on cell banking but may also include some cell engineering. You will be enabling science by acquiring, culturing and banking a large variety of mammalian cells including immortalised cell lines, primary cells and stem cells. The work will also include registration and tracking of cells in databases.

You will be primarily laboratory-based, however you will at times be required to work flexibly across the team to support other tasks.

Responsibilities
• Utilising expertise in cellular biology; independently culture and characterise all types of cells used in drug discovery projects, while incorporating the views of others
• Innovate in the field of cellular biology with a focus on banking and characterisation of cells
• Design and implement work-plans to agreed timelines to meet project objectives, including delivery of more than one agreed area of work in parallel
• Be an effective member of the global cell banking network across AstraZeneca, contributing novel ideas and using judgement and knowledge to influence the cell banking field

Your profile
Essential skills, knowledge & competencies
• PhD in Cell biology, Biotechnology, Biochemistry or a related discipline or a BSc/MSc degree with significant relevant experience, preferably in the pharmaceutical or biotechnology industry
• Expert in cell culturing and banking of a wide range of adherent and suspension mammalian cells; including cell lines, primary cells, iPSCs and stem cells at plate-, flask- and multi-layer cell stack scale
• Skilled in cellular biology techniques used to develop transient and stable cell lines
• Experience with handling of license agreements, material transfer agreements and ethical consents
• Computer literate: articulate, confident and competent in the use of Microsoft Word and Excel, and knowledge in using reagent databases
• Strong organisational and logistic skills

Desired skills
• Experience in working with human biological samples
• Differentiation and reprogramming of iPSCs
• Experience in isolation of primary cells from tissue and/or immortalisation of cells
• Understanding of molecular biology and design of DNA constructs

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we are opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Interested? Come and join our journey.

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Physical Laboratory Engineer

Materialkemist
Läs mer Apr 26
Mölnlycke Health Care is a world-leading provider of single-use surgical and wound care products for customers, healthcare professionals and patients. We develop and bring to market innovative wound care and surgical products along the entire continuum of care – from prevention to post-acute settings. Our solutions provide value for money, supported by clinical and health economic evidence.

About the position
We are now recruiting a Physical Laboratory Engineer within projects and platforms for a consultant assignment that will start in June or after agreement. The purpose of this position is to provide projects, platforms and other customers with physical test data accompanied by documented analysis and statistical input. The work includes a significant amount of setting up systems for testing of wound dressings, and thus require a technical mindset and experience within laboratory work. You will also secure expertise within physical testing for Mölnlycke Health Care.

Applications will be evaluated continously and the position may be filled befor the end date. Submit your CV and personal letter today!

Responsibilities
As a physical laboratory engineer you will be a key player in the day-to-day operations within a regulatory controlled environment.

The work includes, but are not limited to:
*Physical testing to projects and platforms - ensure that physical tests are executed with appropriate methods and that test analyses are delivered in a timely and efficient fashion to support business objectives.
*Setting up systems to test various physical properties.
*Outsourcing - plan, order, follow up execution and secure reports of tests to be performed by external laboratories.
*Implement new methods - responsible for the implementation of new physical test methods.
*Take part in the validation and development of test methods.
*Instruments - control and maintain performance of laboratory equipment and support continuous improvement activities.
*Regulatory demands - analyse tests and report data in accordance with the quality system.
*Participate in the work to maintain the quality system in the laboratory.

Your profile
We expect you to have:
*A Bachelor´s or Master´s degree, preferably in Material Science, Chemical, Textile or Mechanical Engingeering or a similar field.
*Relevant hands-on laboratory experience.
*Test performance skills.
*Equipment and method knowledge within physical testing.
*Collaboration and communication skills.
*Experience from working with cross disciplinary projects.
*Knowledge within regulatory demands.
*Previous experience working in a regulatory controlled environment.
*Previous experience working in the MedTech industry (desirable).


About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you. Being a consultant at QRIOS gives you opportunities to try different industries, companies and roles.

It suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

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Lead Process Engineer

Civilingenjör, process, kemiteknik
Läs mer Apr 29
Are you a Chemical och Mechanical Engineer with great experience from the Process industry? Do you like to work interdisciplinary, utilizing your knowledge and experience in different projects? Then this might be the optimal position for you!

Valmet is now looking for a Lead Process Engineer to join the Gothenburg organization for a long-term contract.

Valmet is a leading global developer and supplier of process technologies, automation and services for the pulp, paper and energy industries. The company has over 220 years of industrial history and a strong track record in continuous improvement and renewal.

Valmet is organized around five business lines and five geographical areas. The business lines are Services, Pulp and Energy, Paper, Automation Systems and Flow Control. The areas are North America, South America, EMEA (Europe, Middle-East and Africa), Asia Pacific, and China. The areas are responsible for sales, providing services that meet customers’ needs and support of project deliveries in their respective regions.

Responsibilities
Your main task will be design and lead process work of Evaporation plants to the Pulp industry, both new plants and rebuilds. You will be designing P&IDs;, make mass and energy balances as well as dimensioning of Process equipment. You will work with Sales projects, Customer order projects as well as R&D projects. In Customer order projects you will participate in commissioning, start-up, test run and inspections of the plants.

Valmet in Gothenburg have the global product responsibility for evaporator technology within Valmet. We work closely together with our market Areas, hence International contacts and travelling will be frequent, e.g. during plant maintenance revision-stops.
The ultimate target is to achieve a satisfied customer with profitable operation of the Valmet equipment.

Your profile
To be successful in this position we expect you to have:
* An an Engineering degree with a major in Chemical or Mechanical Engineering or similar.
* 5-8 years of experience from working as a process engineer.
* Excellent skills in English, spoken and written. Additional languages could be meriting.
* An innovative mind with a problem-solving focus.
* Broad skills in technical calculations.
* An open mind to learn new thing.
* Good presentation skills.

In this role you will be working closely with other process engineers and product experts. You will therefore have to be a good team player, while also being able to find your own paths, both at work and when out travelling.

Does this sound like an interesting opportunity for you? Make sure to submit your application today!

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you. Being a consultant at QRIOS gives you opportunities to try different industries, companies and roles.

It suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.


Please apply by registering your CV here on our website. Click on the "Ansök" button to the right. It is our recommendation that you register as much information as possible and that you attach a complete CV-document. Please check that your correct e-mail address is registered.

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Senior Research Scientist

Forskare, farmakologi
Läs mer Apr 26
Senior Research Scientist – In vitro cardiac disease modelling

Are you an experienced scientist in the field of stem cells and gene editing? Would you like to contribute to the development of novel therapies?

This might be the next challenge for you!

At AstraZeneca in Gothenburg, Sweden we have an exciting opportunity for you to join us in Applied Stem Cell Sciences group in Translational Genomics, Discovery Sciences, Biopharmaceuticals R&D, as a bench-based Senior Research Scientist to be a key player in developing therapeutics to change patients’ lives.


About the position
You will be based in Gothenburg Sweden, working alongside our stem cell scientists, disease area specialists and genome editing group. Using your strong knowledge and experience in stem cell biology, cell model development and CRISPR technology you will have the opportunity to work on in vitro aspects of therapeutic genome editing projects. This includes culture, genome-engineering and differentiation of induced pluripotent stem cells (iPSCs) and genetic and functional validation of engineered lines.

The role is focused on laboratory-based activities. Your biggest impact will be through significant contributions to the practical delivery to projects in compliance with AstraZeneca corporate responsibility, policies and relevant safety standards.

It is essential to have good social and communication skills, be collaborative and a strong team player. Candidates should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude.

Good organizational, data management and documentation skills are required, and you should be comfortable in presenting your results. English language is required, both spoken and in writing.

Responsibilities

• Culture and differentiation of human iPSC lines to cardiac and skeletal muscle
• Perform molecular biology, biochemical, and cellular assays to evaluate the outcomes of gene editing experiments on genomic DNA, mRNA, protein, and functional levels.
• Culture of human primary cells and various mammalian cell lines.
• Effectively collaborate within a matrixed research team to facilitate the success of projects.
• Maintain complete experimental records.


Your profile
•PhD in Developmental Biology, Cell Biology, Gene Editing or a BSc/MSc degree with significant experience
•Proven experience with PSC biology and directed-differentiation to cardiac and/or skeletal muscle
• Demonstrable experience with cell line engineering using CRISPR/CAS9
•Design, develop, and optimize in vitro transfection/transduction experiments using a variety of perturbagens, including lentivirus/AAV-mediated infection
•Hands-on experience with the following assay platforms: RT-qPCR, ddPCR, Flow Cytometry, ELISA, Western blots, and cellular functional assays
•Experience with the culture of multiple mammalian cell types including primary cells
•Excellent communication skills with ability to build open and collaborative relationships and work effectively as a member of a multidisciplinary team
•Excellent organizational skills and documentation practices

The following skills are highly desirable:
• Experience with NGS library prep, bioinformatic analysis, and cutting-edge molecular biology methods
• Expertise with liquid handling automation technologies
• Experience of setting up cell based pharmacological assays

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we are opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Interested? Come and join our journey.

Ansök nu

Analytical Chemist

Analytisk kemist
Läs mer Apr 25
Do you have experience in working with analytical chemistry? Are you driven as a person and good at communicating? Then you might be our new star! We are looking for an Analytical chemist for a long-tearm assignment at AstraZeneca with start as soon as possible.

The process is on going so don´t hesitate to apply to day! We are looking forward to your application!

About the position
At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.

Pharmaceutical Sciences at AstraZeneca deliver the therapies of the future through scientific leadership in drug delivery, design of synthetic routes, and manufacturing of Active Pharmaceutical Ingredients (API) across all the AstraZeneca therapy areas.

Our vision is to be “pharmaceutical science leaders, creating innovative and cost-effective solutions, shaping the diverse therapies of the future”.
We’re looking for talented and motivated analytical chemist to join our analytical and solid state characterization team within Early Product Development and Manufacturing (EPDM) in Gothenburg.

You would join a highly collaborative team and together we will deliver the analytical science to product development within the early portfolio up to phase II.

Responsibilities
This is a lab-based role where you will work collaboratively with colleagues, documenting your experiments carefully and to the right quality. You will get the opportunity to apply your excellent analytical expertise to the drug projects you are working in, contributing to the progression of these projects and drive the scientific development within the field of analytical science at AstraZeneca.


Your profile
To be successful in this role you will need a strong scientific background with good skills in written and verbal communication and the ability to engage and collaborate across boundaries with a positive problem-solving attitude and delivery focus.

Required Qualifications, Skills and Experience:
o University degree (MSc, PhD) in relevant discipline, preferable with industry experience
o Scientific knowledge within analytical science and technically skilled to use chromatography with relevant detection techniques for small molecules
o You are a driven experimentalist, with a passion to deliver highly relevant and reliable data and with the ability to be influential in discussions in a wide set of communities and multi-disciplinary project teams
o Excellent communication, collaboration, networking and leadership skills & ability to lead and inspire colleagues

If you also have experience in one or more of the following areas – great!
o Industry experience of pharmaceutical development including oral solid dosage form development
o Experience of CMC submissions and work according to GMP
o Skilled in specific analytical techniques for small molecules, e.g. mass spectrometry, NMR, dissolution etc
o Track record and keen interest of driving development within analytical science including championing new technologies and solutions

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.

About Astra Zeneca:
AstraZeneca is a major international healthcare company engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we are more than one of the world’s leading pharmaceutical companies - at AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

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Clinical Supply Coordinator

Forskare, farmakologi
Läs mer Apr 19
At AstraZeneca, we believe in the potential of our people and you’ll develop beyond what you thought possible! We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us.

In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.

The Clinical Supply Coordinator (CSC) supports Global Clinical Supply Chain (GCSC) to ensure the delivery of clinical material and associated information to meet the agreed clinical demand. This role is a great opportunity for someone wishing to embark on a career within Supply Chain Management.

About the position
The CSC supports GCSC teams with task-based activities that include:

• Coordination of the ordering of the manufacture of drug substance, drug product and packaged supplies, ensuring timely supply of clinical trial material to patients.
• Management of documentation activities ensuring inspection readiness to meet international GMP standards.
• Timely management of complaints and deviations.
• Utilise Supply Chain Management systems to support agile ways of working.
• Continually improve the Clinical Supply Chain processes through visual management, problem solving, standardisation and process confirmation.


Responsibilities
This role covers parts of the clinical study lifespan, across all phases of the drug development lifecycle, covering small and large molecule drug products.

In this role you will have the opportunity to work with multiple customers and partners internally and externally. You will follow SHE and GMP standards, and will be personally accountable for these areas within your own work plans.

Your profile
• A scientific / business / supply chain degree (or equivalent) with excellent grades
• Thrives in a process orientated workplace, on task based activities and with a focus on the customer.
• Organised and structured with an excellent aptitude for digital systems.
• Team player with a problem solving mindset and a focus on quality.
• Comfortable in a high paced and agile environment

Desirable Requirements
• Demonstrated understanding of the importance of standardised processes and Lean improvement.
• Knowledge of Clinical Manufacturing & Supply and the drug development process.

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we are opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Interested? Come and join our journey.

Ansök nu

SmartSupplies Specialist

Forskare, farmakologi
Läs mer Apr 19
Our Gothenburg site is one of AstraZeneca's three strategic R&D centres. Here, you'll feel a global atmosphere in a multinational environment. Collaboration comes in all forms - across teams, functions, countries and even companies. With more than 2,400 employees from over than 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthrough come together. We believe that the diversity of our people is crucial to bringing new discoveries to life. We value the unexpected ideas or thoughts that come from a chat over something as simple as a warm cup of coffee or a stroll on our “walk and talk” meeting trail.

The Global Clinical Supply Chain (GCSC) function within Clinical Manufacturing & Supply (CM&S) is accountable for the supply of medicines to AstraZeneca’s clinical trials and toxicology studies. Clinical supply chains are amongst the most complex of any industry and our customers are increasingly demanding more speed and agility, as well as management of complex device supply chains and new modalities, without compromising quality or risk, so we need well-managed, fit-for-purpose systems to meet these challenges.

Responsibilities
The SmartSupplies Specialist will perform and support wider Clinical Manufacturing & Supply (CM&S) organization via a variety of responsibilities:
• Create, manage and maintain high quality system and project data
• Support and/or lead system change management and drive improvements including raising, implementing and closing change requests.
• Support Clinical Manufacture and Supply organization with problem solving e.g. resolution of system incidents/problems and provide overall support to CM&S staff.
• The SmartSupplies Specialist has a key role in improvement and validation work in connection to SmartSupplies system (and other GxP systems).
• Develop and implement new technological solutions to help CM&S to operate more efficient and with improved quality. This is essential for AstraZeneca success in the pharmaceutical business.
• Develop and provide training to GCSC and other relevant parties.

Your profile
Essential for the role
• College/university degree in Computing/engineering/science preferred
• Highly numerate, supported by strong computing skills
• A track record of working and managing change in GxP systems or equivalent
• Experience of good documentation practice within system management area
• Experience of URS development and authoring
• Demonstration of high attention to detail, particularly when related to Systems Master Data
• Experience of effective working in a multi-cultural team
• Proven analytical and strategic thinking
• Demonstrated good time and stakeholder management skills & flexibility to adapt to changing customer need
• Excellent English, both verbally and written

Desirable for the role
• Experience of drug substance or drug product development is highly valuable
• Experience of developing standard reports from computer systems
• experience
• Knowledge in performing database searches
• Conceptual thinking and experience of strategic frameworks
• Knowledge of the AZ Clinical Supply Chain systems environment, including SmartSupplies (or equivalent commercial systems eg SAP) and RTSM
• Experience and familiarity with supply chain processes (clinical or commercial)
• Experience of lean / lean leadership / lean thinking
• Experience of agile development

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we are opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Interested? Come and join our journey.

Ansök nu

Regulatory Information Manager

Forskare, farmakologi
Läs mer Apr 19
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

Global Regulatory Operations (GRO) manages several parts of Regulatory Information Management (RIM) within AstraZeneca. GRO has the expertise and provide the tools and services to be able to meet:

• The ever-increasing complexity of regulations and product portfolios
• Growing demand for data due to increased public and regulatory scrutiny
• Global collaboration and standardization of formats and processes across the markets
• Increased use of partners and outsourcing

About the position
The Regulatory Information Manager is primarily responsible for supporting the management, collection, coding and analysis of AstraZeneca regulatory information, the Global Product Registration List and regulatory data standards such as XEVMPD and IDMP.
Typical Accountabilities:
• Manages the collection, coding and analyses of regulatory information for assigned products in accordance with regulatory data standards, quality control and quality improvement methodologies.
• Compiles and delivers XEVMPD or other regulatory information-based submissions to health authorities.
• Develops self in topic areas critical to successful delivery of the RI remit. Particularly, technical skills (XEVMPD, IDMP), knowledge of international regulations and skills (communication, project management).
• Engages with partners, affiliates, subsidiaries or other stakeholders to collect regulatory information and to ensure compliance with procedures and standards.
• Monitors the environment for changes in legislation related to regulatory information.
• Reviews and evaluates regulations, guidelines and technical specifications related to regulatory information processes and regulatory information data standards.
• Identifies opportunities for continuous improvement.
• Prepares business reports or alerts in response to business or health authority request.
• Ensures collection and coding of regulatory information is done in compliance with regulatory and pharmacovigilance legislation, regulatory processes and regulatory data standards.

Your profile
Minimum requirements
• University degree in the life sciences or IT
• Experience in pharmaceutical/medical industry
• Knowledge of pharmaceutical drug development process
• Strong analytical and critical thinking ability
• Good understanding of current regulatory legislation, guidelines and trends relating to regulatory information (process, tools, standards)
• Able to manage productivity responsibilities

Preferred experience and key factors
• Good problem and conflict resolution skills
• Ability to set and manage priorities, performance targets and project initiatives
• Ability to innovate best practices with business process analysis and design
• Ability to thrive in a rapid paced environment

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we are opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Interested? Come and join our journey.

Ansök nu

Quality Assurance Advisor

Forskare, farmakologi
Läs mer Apr 19
AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.

The arena
Are you interested in a challenging opportunity within the Development Quality function in one of the world’s leading pharmaceutical companies?

The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca. We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. AstraZeneca’s pharmaceutical development organizations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase.


About the position
As a Quality Advisor, you will work with early product development manufacturing and packaging teams and be responsible for Development Quality release of externally manufactured Drug Product and Investigational Medicinal Product for clinical trials. You are expected to assure that activities and processes across the development chain are delivered to appropriate standards to meet regulatory expectations and assure product integrity and acceptability.

You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. In your role you will have interactions with internal and external stakeholders.

Responsibilities
Typical Accountabilities:
• Responsible for quality Release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
• Providing quality input to Manufacturing, Packaging, Labelling & Distribution activities
• Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
• Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects
• Provide appropriate Quality Assurance input to business improvement projects
• Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working.

Your profile
Minimum requirements – Education and Experience
• MSc in pharmacy or engineering (specializing in Pharmaceuticals) with at least 3 years’ experience of working within a pharmaceutical GMP environment
• Broad understanding of Quality Systems and GMP and related activities to Investigational Medicinal Product (IMP)
• Comprehensive understanding of the pharmaceutical/drug development process
• Good communicator with experience of interacting effectively across interfaces
• Understanding of Project Management processes
• Fluent in written and spoken English

Preferred requirements
• Experience preferably within a pharmaceutical manufacturing organization
• Good team working and networking skills
• Capable of making effective decisions
• Demonstrate drive and energy in the role to make a difference
• Demonstrate a high degree of personal credibility

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we are opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Interested? Come and join our journey.

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Drug Product Delivery Operator

Forskare, farmakologi
Läs mer Apr 19
We are curious, creative, and open to new ideas and ways of working. Above all, we are passionate about science and driven to always put patients first. Join AstraZeneca and apply your expertise in a company that are following the science and turn ideas into life changing medicines. We have an exciting opportunity for talented DPD Operators to be based in Gothenburg, Sweden.

Drug Product Delivery (DPD) within Pharmaceutical Technology & Development is the sole internal AstraZeneca department that packs, labels and distributes investigational medicinal products to clinical trial patients. We support launched, pre-launched and products under development within all our therapeutic areas. We work in a fast paced environment where flexibility and agility enable us to deliver high value to early phase clinical trials.

About the position
The DPD Operator role will be a flexible role within Drug Product Deliveries three operational skill areas, Material Management, Pack Label and Distribution. We work in a environment where flexibility and agility enable us to deliver high value to early phase clinical trials. To complement our existing team, candidates with the following experiences is of interest:

- Distribution experience from a complex supply chain organization
- Knowledge / expertise in working with automated/semi-automated equipment in an operational environment
- Drug Product Knowledge including management of Item/article and lot/batch management to ensure traceability on items/articles in a patient kit including a drug product, packaging material and patient labels from the pharmaceutical industry

Responsibilities
Main Duties and Responsibilities
The role holder will contribute to the DPD organization applying their expertise in the complex and regulated GMP environment. The work is focused on being flexible and operational within at least two skills. As a DPD operator you will perform and document all the operational work according to written procedures. Be engaged in the development and improvement of internal processes and manage deviations. Be responsible for writing of GMP and SHE procedures within own skill areas and will be responsible for related training and compliance activities. As required maintain defined facilities or equipment according to GMP standards and be proactive to contribute to projects/activities through applying specialist knowledge within appropriate areas.
Material Management & Distribution responsibilities example
Preparing documentation, receiving and packing of investigational medicinal products to clinical trials. Being the main point of contact when it comes to distribution questions for a number of studies.
Pack & Label responsibilities example
Handling batch documentation, primary pack(tablets or capsules in bottles) and secondary pack(labeling of bottles, devices and vials). Being responsible for equipment (manual and automated) including instructions, training, qualification etc.

Your profile
Essential requirements and skills
? BSc/MSc in chemistry/pharmacy/engineering or equivalent experience. Preferably 2 years experience within pharmaceutical development
? Demonstrated ability to work with teams in a culturally diverse, complex and changing environment most internally but to some extent externally
? Curious and innovative mindset with problem solving ability - resolve issues with minimal guidance
? Good written and verbal English communication and understanding

Beneficial requirements and skills
Understanding of principles, applications and management of SHE and GMP in an R&D environment
? Understanding the disciplines in Drug Product Delivery, Supply Chain and Pharmaceutical development in order to contribute to an effective Supply Chain organization

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Tekniker inom luftfart till Landvetter flygplats

Servicetekniker, elektronik
Läs mer Apr 1
Är du en ansvarstagande person med starkt teknikintresse? Vi på AVISEQ Critical Communication AB söker nu en tekniker inom luftfart till Landvetter flygplats.

Om tjänsten
I rollen som tekniker erbjuds du ett utmanande och stimulerande arbete i en spännande miljö inom vår luftfartsenhet med inriktning på flygledningssystem, kommunikations-, navigations- och surveillance system (CNS) samt terminalsystem. Du kommer att vara en viktig länk i kedjan att upprätthålla den tekniska säkerheten kring luftfarten och flygtrafiken. Vidare är du ansvarig för att säkerhetsställa att arbetet bedrivs enligt gällande kvalitets- och miljöanvisningar.

Dina arbetsuppgifter i huvudsak
Arbetet innefattar förebyggande och felavhjälpande underhåll av följande system:
• Flygledningssystem
• Navigationssystem
• Radio
• Radar
• Meteorologisk utrustning
• Kommunikationssystem
• IP Nätverk och PC-applikationer
• Publika system i terminalbyggnader

Flertalet av systemen på flygplatsen är av unik karaktär. Därför kommer du som tekniker att genomgå en grundutbildning och ett antal specifika påbyggnadskurser. Du får arbeta på ett företag som är en ledare inom sin bransch och du blir en del av ett team som består av ambitiösa och engagerade kollegor.
Det ingår resor i arbetet då vi även har utrustning utanför flygplatsen och på närliggande flygplatser. Du kommer tillhöra ett team om 10 Serviceingenjörer på Landvetter flygplats och ett större team som omfattar hela södra Sverige. Du kommer att ingå i en beredskapslista med schemalagd arbetstid.


Vem är du?
För att trivas med och lyckas i rollen som Tekniker på AVISEQ är du självständig och drivande men har samtidigt lätt för att samarbeta, både med kollegor och med våra kunder. Du har en kreativ och lösningsorienterad inställning till hur du utför ditt arbete och du har ett brinnande teknikintresse.

Vi tror att du har minst 3-årig teknisk gymnasieutbildning eller en högskoleingenjörsutbildning alternativt en motsvarande relevant arbetslivserfarenhet. Vi ser gärna att du har yrkeserfarenhet och kunskaper om radioteknik, analog/digital elektronik, mekanik samt erfarenhet av underhåll på teletekniska system. Erfarenhet av förekommande utrustning och instrument samt PC-baserade stödsystem är starkt meriterande. Du har en god kommunikativ förmåga i svenska och engelska. Du har B-körkort.


Om verksamheten
AVISEQ verkar inom kritisk kommunikation. Vi är specialister på att erbjuda kostnadseffektiva tjänster utan att göra avkall på säkerheten. Vi övervakar, driftar och underhåller våra kunders tekniska utrustning och system, allt för att säkerställa deras kritiska verksamhet. Våra största kunder verkar inom luftfart och säkerhet vid flygtrafikcentraler, flygplatser, statliga myndigheter och företag, såväl offentliga som privata, i hela Sverige. AVISEQ har cirka 200 anställda och blev i maj 2020 en del av LFV-koncernen. Vi vill vara den bästa arbetsplatsen för dig som gillar utmaningar och att ta ett samhällsansvar!

Tjänsten är en tillsvidareanställning på 100%, där vi tillämpar 6 månaders provanställning. Grund för anställning är godkänd registerkontroll/säkerhetsprövning och tillträde sker enligt överenskommelse.

Urval sker löpande, så ansök nu.

För mer information besök gärna https://aviseq.se/

#LI-HG1

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Team Manager - Automotive

Gruppchef, teknik
Läs mer Mar 30
Do you have high energy and passion for leadership, recruitment, and sales, along with development of strategies and a genuine interest for engineering technologies? Are you the future leader we are looking for, to lead our Interior & Exterior team within Business Unit Engineering?

As a Team Manager you will be part of a global organization where you will have the entire Profit and Loss responsibility for the Interior and Exterior team. Our goal is to continue developing our leading position, where we help our customers to transform their products and services by co-creating point solutions, platforms & systems. Our core values Ambition & Care influence everything that we do, and we will always put our employees first.

About the position
In this role, you will lead a fast-growing team and make sure that we offer our key clients the best solutions and competence. As a Team Manager you have the full responsibility for your team, including Profit & Loss, and for the operations with your resources. You are also deeply motivated by engaging your employees, making sure that their competence gets the best possible development.

You have a genuine interest in automotive industry, with knowledge in Engineering, Function/Platform Development Processes or similar. You will create customer solutions to develop our in-house projects, which we deliver to our customers within the domain. You will be responsible for building your own team-specific competence and for allocating resources, while developing your team and environment.

Sales & Customer Relations are key components, and should enjoy the daily discussions with new and existing customers. You also ensure profitability and growth of your team through recruiting – and keeping – the right employees.

Responsibilities
As a Team Manager at Capgemini Engineering, you are the heart and soul of our company. You know what to deliver, regardless whether it is a local or global project or service.

Furthermore the role involves but are not limited to:

• Ensure the profitability of your team, while managing your employees
• Staffs your employees on best projects & assignments
• Drive and set your sales strategy and build customer relations
• Take responsibility of creating and meet agreed budget
• Collaborate with our Talent team, to recruit the right talents
• Follow the company and unit strategy
• Anticipate contract ends and resources reallocation
• Manage and support career development for your team
• Contribute to R&D projects / offers development
• Ensure renewals and upsell on your territory
• Work on technical client proposals

Your profile
In order to be successful in the role weexpect you to have the following background:

Experience
• Background from Mechanical Engineering within Automotive
• Experience from sales (preferably B2B)
• Experience preferably as a Team Manager or other leading roles (Project Manager, Product Owner, Scrum Master or similar)
• Experience from consulting business
• Fluent in English and Swedish

Personal qualities
• Quick-footed and flexible
• Structured and methodical
• People's person and service oriented
• Result-oriented person who loves to drive and execute strategy

It is a merit to have experience from project leadership and working in an international context.

Do you see yourself as a structured person with the heart in the right place. Prestige has no room at Capgemini Engineering. You are ambitious and you always strive to do “bigger and better” – a fearless go-getter with an easy going personality, and close to laughter.

Is this you? Perfect, we´re looking forward to meeting you!

We are interviewing candidates on a continuous basis and welcome your application today.


About the organisation
QRIOS Life Science & Engineering can offer several opportunities for skilled people with a background in engineering or science. We work with Sweden’s leading pharmaceutical and life science and engineering companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.

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Quality Advisor

Forskare, farmakologi
Läs mer Apr 14
We are searching for a Quality Assurance Advisor for a global pharmaceutical company.
As a Quality Advisor, you will work with early product development manufacturing and packaging teams and be responsible for Development Quality release of internally or externally manufactured Drug Product and Investigational Medicinal Product for clinical trials.
You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. In your role you will have interactions with internal and external stakeholders.


Responsibilities
• Responsible for quality Release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
• Providing quality input to Manufacturing, Packaging, Labelling & Distribution activities
• Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards
• Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects
• Providing quality advice and approval of documentation related to equipments, facilities, IT systems and instruments e.g. maintenance, calibration, validation and change control
• Provide appropriate Quality Assurance input to business improvement projects



Your profile
• MSc in pharmacy or engineering (specializing in Pharmaceuticals) with at least 3 years’ experience of working within a pharmaceutical GMP environment
• Broad understanding of Quality Systems and GMP and related activities to Investigational Medicinal Product (IMP)
• Comprehensive understanding of the pharmaceutical/drug development process
• Good communicator with experience of interacting effectively across interfaces
• Understanding of Project Management processes
• Fluent in written and spoken English


About the organisation
This position is a consultant assignment at our client via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

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Affärsutvecklare - datadrivna insikter och organisationsutveckling

Affärsutvecklare
Läs mer Mar 10
Om tjänsten
Vill du skapa förutsättningar för verksamheter att bli mer datadrivna i sina beslut?
Nu söker vi en Affärsutvecklare/Managementkonsult för en spännande utmaning att starta och utveckla ett nytt verksamhetsområde inom datadrivna insikter, organisationsutveckling och management.

QRIOS Minds Insights AB är ett nystartat dotterbolag i Pooliakoncernen.
Uppdraget är att förse koncernen och våra kunder med datadrivna insikter som kan användas som beslutsunderlag, samt att sälja och leverera tjänster inom organisationsutveckling och management.

Rollen innebär att självständigt och i samråd med koncernledningen bygga upp verksamheten. Du axlar rollen som VD för dotterbolaget och har då också resultatansvar.

Delägarskap är en möjlighet som vi vill att du känner dig inspirerad av. Är ni flera som vill vara med på denna spännande resa ser vi det bara som en fördel!

Vi erbjuder en inkluderande och varm företagsmiljö med ett starkt varumärke i en koncern som är i en expansiv och kreativ fas. Givetvis är även det affärsmässiga och det ekonomiska resultatet viktigt.

Ansök redan idag via
https://workspacerecruit.com/lediga-jobb/affarsutvecklare-datadrivna-insikter-och-organisationsutveckling/

Dina arbetsuppgifter i huvudsak
•Framtagande av Insights från kunder, kandidater och konsulter. Det görs genom befintliga men även nya system som du kommer upphandla och/eller utveckla ihop med Koncernledningen. Exempel på material kan vara framtidsrapporter, karriärrapporter och annat som ger mervärde för våra kunder eller vår verksamhet.

•Försäljning av framtagna Insights till befintliga och nya kunder tillsammans med övriga koncernen.

•Införsäljning och genomförande av tjänster inom organisationsutveckling och management

•Konceptualisering och införsäljning av HR-tjänster såsom Onboarding och Employer Branding

•Vid sidan av projektleverans och försäljning innebär rollen även att vara intern förändringsledare och tillsammans med dina kollegor utveckla Pooliakoncernens erbjudande, implementera nya strategier, system och processer samt att coacha medarbetare att lyfta sitt eget arbete till en mer insiktsdriven nivå.

Vem är du?
Vi söker dig som har en bakgrund inom t.ex. HR, Management Consulting, Rekryteringsbranschen och försäljning. Du har en för tjänsten relevant akademisk examen. Det är starkt meriterande om du har erfarenhet av att ta fram data och paketera det till värdeskapande insikter och kunna ge konkreta exempel på tidigare leveranser.

Som person har du ett starkt eget driv, är både sälj- och leveransinriktad och har förmåga att se kundens behov. Affärsmässighet är en förutsättning för att kunna skapa ett lönsamt tjänsteområde.

Du gillar att tänka och arbeta både operationellt och strategiskt. Du är analytisk och strukturerad med förmåga att kunna förstå och bryta ner affärsproblem.

För att lyckas i rollen behöver du även kunna prata och skriva svenska på en professionell nivå, engelska på hög nivå, samt ha god vana att presentera.

Ansök redan idag via:
https://workspacerecruit.com/lediga-jobb/affarsutvecklare-datadrivna-insikter-och-organisationsutveckling/

Om verksamheten
QRIOS Minds Insights är en del av Pooliakoncernen och bedriver verksamhet inom Management Consulting. Vi är starkt inspirerade av dem som aldrig slutar leta efter nya lösningar. Som vi säger, QRIOS MINDS GO FURTHER.
Pooliakoncernen har ett heltäckande erbjudande med konsulttjänster och rekryteringstjänster från QRIOS, bemanning och rekrytering från Poolia och Uniflex samt HR-Tech tjänster från Roi Rekrytering och Workspace Recruit.

Anställningsort: Stockholm, Göteborg eller Malmö

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Lead Process Engineer

Processingenjör, kemiteknik
Läs mer Apr 11
Are you a Chemical och Mechanical Engineer with great experience from the Process industry? Do you like to work interdisciplinary, utilizing your knowledge and experience in different projects? Then this might be the optimal position for you!

Valmet is now looking for a Lead Process Engineer to join the Gothenburg organization for a long-term contract.

About the position
Valmet is a leading global developer and supplier of process technologies, automation and services for the pulp, paper and energy industries. The company has over 220 years of industrial history and a strong track record in continuous improvement and renewal.

Valmet is organized around five business lines and five geographical areas. The business lines are Services, Pulp and Energy, Paper, Automation Systems and Flow Control. The areas are North America, South America, EMEA (Europe, Middle-East and Africa), Asia Pacific, and China. The areas are responsible for sales, providing services that meet customers’ needs and support of project deliveries in their respective regions.

Valmet is an established market leader and has a strong market position in all its businesses.

Responsibilities
Your main task will be design and lead process work of Evaporation plants to the Pulp industry, both new plants and rebuilds. You will be designing P&IDs;, make mass and energy balances as well as dimensioning of Process equipment. You will work with Sales projects, Customer order projects as well as R&D projects. In Customer order projects you will participate in commissioning, start-up, test run and inspections of the plants.

Valmet in Gothenburg have the global product responsibility for evaporator technology within Valmet. We work closely together with our market Areas, hence International contacts and travelling will be frequent, e.g. during plant maintenance revision-stops.
The ultimate target is to achieve a satisfied customer with profitable operation of the Valmet equipment.

Your profile
To be successful in this position we expect you to have:
* An an Engineering degree with a major in Chemical or Mechanical Engineering or similar.
* 5-8 years of experience from working as a process engineer.
* Excellent skills in English, spoken and written. Additional languages could be meriting.
* An innovative mind with a problem-solving focus.
* Broad skills in technical calculations.
* An open mind to learn new thing.
* Good presentation skills.

In this role you will be working closely with other process engineers and product experts. You will therefore have to be a good team player, while also being able to find your own paths, both at work and when out travelling.

Does this sound like an interesting opportunity for you? Make sure to submit your application today!

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you. Being a consultant at QRIOS gives you opportunities to try different industries, companies and roles.

It suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.


Please apply by registering your CV here on our website. Click on the "Ansök" button to the right. It is our recommendation that you register as much information as possible and that you attach a complete CV-document. Please check that your correct e-mail address is registered.

Ansök nu

Process Engineer

Processingenjör, kemiteknik
Läs mer Apr 11
Are you a Chemical och Mechanical Engineer with great experience from the Process industry? Do you like to work interdisciplinary, utilizing your knowledge and experience in different projects? Then this might be the optimal position for you!

Valmet is now looking for a Lead Process Engineer to join the Gothenburg organization for a long-term contract.

Valmet is a leading global developer and supplier of process technologies, automation and services for the pulp, paper and energy industries. The company has over 220 years of industrial history and a strong track record in continuous improvement and renewal.

Valmet is organized around five business lines and five geographical areas. The business lines are Services, Pulp and Energy, Paper, Automation Systems and Flow Control. The areas are North America, South America, EMEA (Europe, Middle-East and Africa), Asia Pacific, and China. The areas are responsible for sales, providing services that meet customers’ needs and support of project deliveries in their respective regions.

Responsibilities
Your main task will be design and lead process work of Evaporation plants to the Pulp industry, both new plants and rebuilds. You will be designing P&IDs;, make mass and energy balances as well as dimensioning of Process equipment. You will work with Sales projects, Customer order projects as well as R&D projects. In Customer order projects you will participate in commissioning, start-up, test run and inspections of the plants.

Valmet in Gothenburg have the global product responsibility for evaporator technology within Valmet. We work closely together with our market Areas, hence International contacts and travelling will be frequent, e.g. during plant maintenance revision-stops.
The ultimate target is to achieve a satisfied customer with profitable operation of the Valmet equipment.

Your profile
To be successful in this position we expect you to have:
* An an Engineering degree with a major in Chemical or Mechanical Engineering or similar.
* 2-5 years of experience from working as a process engineer.
* Excellent skills in English, spoken and written. Additional languages could be meriting.
* An innovative mind with a problem-solving focus.
* Broad skills in technical calculations.
* An open mind to learn new thing.
* Good presentation skills.

In this role you will be working closely with other process engineers and product experts. You will therefore have to be a good team player, while also being able to find your own paths, both at work and when out travelling.

Does this sound like an interesting opportunity for you? Make sure to submit your application today!

About the organisation
QRIOS Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden’s leading pharmaceutical and life science companies. So whether you’re interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you. Being a consultant at QRIOS gives you opportunities to try different industries, companies and roles.

It suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you’re looking for a world of exciting assignments and new contacts, you’ll like being a consultant.


Please apply by registering your CV here on our website. Click on the "Ansök" button to the right. It is our recommendation that you register as much information as possible and that you attach a complete CV-document. Please check that your correct e-mail address is registered.

Ansök nu

Affärsutvecklare - datadrivna insikter och organisationsutveckling

Affärsutvecklare
Läs mer Mar 10
Om tjänsten
Vill du skapa förutsättningar för verksamheter att bli mer datadrivna i sina beslut?
Nu söker vi en Affärsutvecklare/Managementkonsult för en spännande utmaning att starta och utveckla ett nytt verksamhetsområde inom datadrivna insikter, organisationsutveckling och management.

QRIOS Minds Insights AB är ett nystartat dotterbolag i Pooliakoncernen.
Uppdraget är att förse koncernen och våra kunder med datadrivna insikter som kan användas som beslutsunderlag, samt att sälja och leverera tjänster inom organisationsutveckling och management.

Rollen innebär att självständigt och i samråd med koncernledningen bygga upp verksamheten. Du axlar rollen som VD för dotterbolaget och har då också resultatansvar.

Delägarskap är en möjlighet som vi vill att du känner dig inspirerad av. Är ni flera som vill vara med på denna spännande resa ser vi det bara som en fördel!

Vi erbjuder en inkluderande och varm företagsmiljö med ett starkt varumärke i en koncern som är i en expansiv och kreativ fas. Givetvis är även det affärsmässiga och det ekonomiska resultatet viktigt.

Ansök redan idag via
https://workspacerecruit.com/lediga-jobb/affarsutvecklare-datadrivna-insikter-och-organisationsutveckling/

Dina arbetsuppgifter i huvudsak
•Framtagande av Insights från kunder, kandidater och konsulter. Det görs genom befintliga men även nya system som du kommer upphandla och/eller utveckla ihop med Koncernledningen. Exempel på material kan vara framtidsrapporter, karriärrapporter och annat som ger mervärde för våra kunder eller vår verksamhet.

•Försäljning av framtagna Insights till befintliga och nya kunder tillsammans med övriga koncernen.

•Införsäljning och genomförande av tjänster inom organisationsutveckling och management

•Konceptualisering och införsäljning av HR-tjänster såsom Onboarding och Employer Branding

•Vid sidan av projektleverans och försäljning innebär rollen även att vara intern förändringsledare och tillsammans med dina kollegor utveckla Pooliakoncernens erbjudande, implementera nya strategier, system och processer samt att coacha medarbetare att lyfta sitt eget arbete till en mer insiktsdriven nivå.

Vem är du?
Vi söker dig som har en bakgrund inom t.ex. HR, Management Consulting, Rekryteringsbranschen och försäljning. Du har en för tjänsten relevant akademisk examen. Det är starkt meriterande om du har erfarenhet av att ta fram data och paketera det till värdeskapande insikter och kunna ge konkreta exempel på tidigare leveranser.

Som person har du ett starkt eget driv, är både sälj- och leveransinriktad och har förmåga att se kundens behov. Affärsmässighet är en förutsättning för att kunna skapa ett lönsamt tjänsteområde.

Du gillar att tänka och arbeta både operationellt och strategiskt. Du är analytisk och strukturerad med förmåga att kunna förstå och bryta ner affärsproblem.

För att lyckas i rollen behöver du även kunna prata och skriva svenska på en professionell nivå, engelska på hög nivå, samt ha god vana att presentera.

Om verksamheten
QRIOS Minds Insights är en del av Pooliakoncernen och bedriver verksamhet inom Management Consulting. Vi är starkt inspirerade av dem som aldrig slutar leta efter nya lösningar. Som vi säger, QRIOS MINDS GO FURTHER.
Pooliakoncernen har ett heltäckande erbjudande med konsulttjänster och rekryteringstjänster från QRIOS, bemanning och rekrytering från Poolia och Uniflex samt HR-Tech tjänster från Roi Rekrytering och Workspace Recruit.

Anställningsort: Stockholm, Göteborg eller Malmö

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Clinical Research Associate (CRA)

Biomedicinare
Läs mer Mar 21
Är du en person som ser glädje och betydelse i ditt dagliga arbete? Är du redo att med stolthet ta dig an en roll där ditt arbete kommer ha en direkt påverkan på människors hälsa och välbefinnande? Vill du jobba i ett bolag som värdesätter utveckling och rörelse framåt, både på ett professionellt och personligt plan?

På Scandinavian CRO (SCRO) arbetar samtliga medarbetare utifrån tre starka värdeord som präglar hela organisationen: GLÄDJE, STOLTHET och RÖRELSE.

Om tjänsten
SCRO söker nu en Clinical Research Associate (CRA) till sin växande organisation med placering i Göteborg. Som CRA kommer du få möjligheten att bli en del av ett sammansvetsat nationellt team av erfarna kollegor i en expanderande organisation som stöttar den personliga utvecklingen hos varje medarbetare.

Dina arbetsuppgifter i huvudsak
I din roll som CRA kommer du att samarbeta med forskningskliniker främst i södra delen av Sverige där du kommer att vara involverad i alla olika delar av en klinisk studie, både i planeringsfas med ansökningar, site selection, initiation visits samt under studiens gång med bl a monitorering och allmän support till klinikerna. Som CRA är du en viktig nyckelperson under hela studiens gång för att säkerställa att studier utförs enligt studieprotokoll, SOPar, ICH-GCP och andra relevanta regelverk.

Vem är du?
Vi ser gärna att du:
• Har en akademisk utbildning inom Life Science, exempelvis som farmaceut, sjuksköterska eller biomedicinare.
• Minst 2 års erfarenhet i rollen som CRA eller i liknande roller där du har jobbat med monitorering av kliniska studier.
• Erfarenhet inom MedTech och Pharma.
• Utmärkta kunskaper inom ICH-GCP.
• Kännedom om regelverk för medicintekniska produkter (ISO 14155).
• Svenska och engelska flytande i tal och skrift.

För att lyckas i rollen som CRA tror vi att du är:
• Lösningsorienterad med resultatet i fokus.
• En lagspelare som uppskattar att arbeta i team men är trygg i att driva egna projekt.
• En strukturerad och organiserad person.
• Flexibel med en entusiasm att utvecklas och lära nytt.
• IT-orienterad.
• Är positiv till visst resande i tjänsten.


Om verksamheten
SCRO är en full-service kontraktforskningsorganisation (CRO) med en bred erfarenhet av att stötta vården, akademien och industrin med kliniska prövningar. Bolaget har idag cirka 25 anställda med kontor i Uppsala och Göteborg. SCRO har ett nätverk med mer än 130 kunder och har genom åren bidragit till över 350 kliniska projekt. Med en passion för att driva forskning och utveckling inom Pharma och MedTech, såväl som inom akademien, stöttar SCRO sina kunder med att omvandla idéer till verklighet med fokus på att möjliggöra en bättre hälsa för människor.


I denna rekryteringsprocess har SCRO valt att samarbeta med QRIOS Life Science & Engineering. För frågor angående tjänsten är ni välkomna att höra av er till Robin Öz. Urvalet sker löpande och tjänsten kan komma att tillsättas innan sista ansökningsdag. Se därför till att skicka in din ansökan redan idag!

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Senior Research Scientist: Cellular assay development

Forskare, farmakologi
Läs mer Apr 4
At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with integrity even in difficult situations because we are committed to doing the right thing. We continuously pursue world-class medicines in new ways, combining our people’s exceptional skills with those of people from all over the globe.


About the position
As a Senior Research Scientist in cellular assay development in Gothenburg, Sweden, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. You will work within Discovery Sciences, part of AstraZeneca’s BioPharmaceuticals organisation, which focuses on scientific advances in drug discovery across therapeutic areas including, respiratory and inflammation (R&I) and cardiovascular and metabolism (CVRM).
We have an exciting opportunity for you to join us as a lab-based scientist to develop state-of-the-art cell-based screening assays. These assays will be used to support discovery of therapeutic peptides and oligonucleotides in AstraZeneca’s drug discovery pipeline.
To be successful in the role as Senior Research Scientist we believe you are a highly motivated scientist with a passion to make a difference for patients. We see you as a person who enjoys collaboration and team working, who holds networking skills with experience of interacting effectively across interfaces of functions, disciplines, and cultures. This goes hand in hand with strong delivery focus, problem-solving and communication skills.


Your profile
• PhD in Biology, Pharmacology, Cell biology or a related discipline or a BSc/MSc degree with significant relevant experience, preferably in the pharmaceutical or biotechnology industry
• Strong experience in cell biology techniques applied to development of physiologically relevant cellular assays
• A practical understanding of a wide range of cellular assay methods and technologies including qPCR and imaging applied to compound profiling and screening
• Excellent communication skills and an ability to operate effectively in a multi-disciplinary research environment
• Ability to independently analyse and evaluate complex data and deliver data to agreed timelines

Desirable Requirements
• Expertise in the design, development and validation of cellular assays for compound screening and profiling, including peptides and oligonucleotides
• Experience with automation of cell assays, e.g. work with liquid handlers like Echo, BRAVO, CyBi well or Dragonfly
• Experience with design of experiments and statistical analysis of assay performance
• Track record of identifying and adopting scientific and technical advances
• Excellent problem-solving skills, not limited to own area of expertise

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

Why AstraZeneca?
Our Gothenburg site is one of AstraZeneca's three strategic R&D centers. With more than 2,400 employees from over than 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthrough come together. We believe that the diversity of our people is crucial to bringing new discoveries to life.

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Vikarierande Konsultchef till QRIOS Life Science & Engineering

HR-konsult/PA-konsult
Läs mer Mar 29
Om tjänsten
Det är väldigt sällsynt att en sådan här riktig utmaning ramlar ner på det här sättet. En av våra fantastiska medarbetare väntar tillökning och därför letar vi efter någon som kan axla ansvaret för en otrolig viktig del av vår verksamhet under ett år. Vi söker nu en driven konsultchef som vill vara med och utveckla vår nya och expansiva verksamhet i Göteborg!

Du ingår i vårt dotterbolag QRIOS Life Science & Engineering som är en del av Pooliakoncernen och kommer att arbeta tillsammans med rekryterare, laboratorieingenjörer, konsultchefer, forskare, rekryteringskonsulter, kemister, säljare, ja listan är lång över oss alla som samarbetar för att lyckas!




Dina arbetsuppgifter i huvudsak
I den här rollen är du en otroligt viktig person för många av oss som är ute på uppdrag hos våra kunder. Arbetsuppgifterna är varierande men framförallt är det du som är spindeln i nätet för alla oss konsulter som dagligen hjälper våra kunder att lyckas med sin verksamhet.

Du kommer ansvara för allt ifrån onboarding av nya medarbetare, tidrapportering, arbetsrättsliga frågor, arrangera sociala aktiviteter till uppföljning av det viktiga arbete som vi utför hos våra kunder. Genom regelbunden kontakt kommer du säkerställa att våra kunder får den servicen de behöver och därmed kan planera kompetensbehoven för sin framtida verksamhet.

Som en del av Management-teamet i Göteborg jobbar du nära rekryterings- och säljteamen och bidrar till att knyta kontakter med kunder och nya nyfikna talanger till våra kundteam. Vi är en flexibel arbetsplats där den ena dagen sällan är den andra lik vilket ställer krav på oss att vara kreativa och lösningsorienterade. Detta är ett perfekt jobb för dig som tyckte att det var tråkigt att sitta hemma framför Teams under pandemin och längtar efter att få komma ut och träffa folk på riktigt igen!

Vem är du?
Det är en stor fördel om du har erfarenhet inom konsultbranschen sedan tidigare och plus i kanten om det varit inom Life Science- eller tekniksektorn. Har du utfört liknande arbetsuppgifter tidigare så är det också väldigt meriterande. Förutom detta så kommer din nyfikenhet och ditt driv vara det som avgör om du passar in i vårt Göteborgsteam.

Du behöver behärska svenska helt obehindrat och vara bekväm med att skriva och tala engelska.

Låter detta som ett utmärkt jobb för dig? Tveka inte höra av dig till mig om du har några frågor eller funderingar! Vi tillämpar löpande urval så passa på att skicka in din ansökan redan idag!

Om verksamheten
På QRIOS jobbar nyfikna experter inom Life Science, Engineering och IT som vill fortsätta attrahera de bästa medarbetarna, för att kunna fortsätta hjälpa våra samarbetspartners med den viktiga kompetens de efterfrågar. Vi är ett konsult- och rekryteringsföretag som är starkt inspirerade av dem som aldrig slutar leta efter nya lösningar.

Som vi säger, QRIOS MINDS GO FURTHER.

Besök vår hemsida www.qrios.se eller kontakta oss direkt för att få veta mer om vilka vi är och varför just du ska söka dig till oss.

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Logistics Specialist

Logistiker
Läs mer Apr 6
At Nouryon, you are a part of making everyday life easier for people around the world. Without seeing it, you meet us every day in your everyday life. We are in your soles, in your mobile and in the newspaper you read. With a common commitment to innovation, sustainability and safety, our employees work daily for a sustainable future.

We are searching for a consultant that has experience in logistics or supply chain and is fluent in Swedish for a assignment as a Logistics Specialist at Nouryon in Gothenburg!

About the position
As Logistics Specialist you will be responsible for completion of daily modal logistics activities including shipment planning, execution, monitoring, and reporting for assigned respective mode of transport in alignment with cost and service target.

You will be responsible for performing transportation planning, executing, and monitoring for the modal transportation mode according to the defined processes. You will conduct activities including capacity planning, shipment and fleet planning, carrier selection, routing, scheduling, tendering, load building as well as regular transportation bookings.

As a team we are also responsible for the invoicing process and that our vendors are correctly invoiced and that surcharges are managed properly. Most of our activities are handled in a so called TMS (Transporeon) where we have different options and possibilities to optimize shipment cost using functionalities such as, best bid and spot bids etc.

Another important aspect of the job is monitoring and control of all shipments and transactions we are involved in and resolve exceptions as they arise.
We are constantly working on improvements both internally, for our processes and externally, together with our logistics providers where we follow up on set KPI’s and cost performance.

In this role you will be the spider in the web communicating with many different stakeholders such as, site logistics, carriers, customer service, business planning and sales. No two days are alike.

Your profile
Experience in logistics / supply chain. Experience with chemical companies is preferred
Demonstrated knowledge in performing logistics activities
Demonstrated ability to troubleshoot and quickly develop a solution
Experience with carrier relationship management and performance evaluations
Understanding of the modal transport market
Working knowledge and history of using computers and programs specific to logistics (SAP, TMS, WMS) and to general business management (MS Excel, Word)
Language: Swedish and English both written and spoken


About the organisation
This is a consultant assignement at Nouryon in Gothenburg until 2022-12-31. During this time you will be hired by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

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Ingenjör skydd, Ringhals

Skyddsingenjör
Läs mer Mar 7
Om tjänsten
Vill du vara med och bidra till Sveriges fossilfria elförsörjning?

Nu har du möjlighet att göra det hos oss på Ringhals. Vi arbetar tillsammans för att göra Sverige fossilfritt inom en generation. För att nå vårt mål behöver vi engagerade medarbetare som vill arbeta hos en av Sveriges största elproducenter och samtidigt bidra till ett bättre klimat på vår planet.

Vi är övertygade om att mångfald berikar, och arbetar därför kontinuerligt för jämställdhet och inkludering på vår arbetsplats. Läs gärna mer om vårt arbete inom mångfald och inkludering på vår hemsida https://careers.vattenfall.com/se/jobba-med-oss/

Är du intresserad av strålning och dess påverkan på människan, anläggningen och omgivningen samt har viljan och intresset att agera som skyddsbarriär på Ringhals? Som Ingenjör Skydd kommer du att arbeta inom området operativ skydd, vilket innefattar både strålskydd och arbetsmiljö.

Dina arbetsuppgifter i huvudsak
Arbetet spänner över alla verksamheter och innebär bl.a.:
• Självständigt skyddsarbete samt övervakning och kontroll av stationens status och inre miljö ur skyddssynpunkt.
• Du kommer att samverka med utförare genom att planera enskilda arbeten samt medverka i projekt och större underhållsarbeten.
• Agera som internutbildare i vissa strålskyddsutbildningar.
• Dokumentationsansvar som innebär att du kommer att få arbeta med att ta fram, implementera och förvalta rutiner för vår verksamhet. Vidare så får du ett övergripande ansvar för att säkerställa att arbetet dokumenteras, och att det sker på rätt sätt.

Vem är du?
Vi söker dig som har:

• Minst 3-årig gymnasieutbildning
• Strålskyddsutbildning eller motsvarande kunskap
• Arbetslivserfarenhet från drift, underhåll eller skyddsverksamhet inom kärnkraftindustrin
• Flytande i svenska både i tal och skrift, goda kunskaper i engelska.

Arbetet innebär mycket frihet under ansvar varför du behöver vara självgående, noggrann och serviceinriktad. För att kunna bidra till enhetens utveckling vill vi att du är kreativ, lyhörd och positiv till förändringar. Det är även viktigt att du tycker om att arbeta i grupp och vill bidra i vårt gränsöverskridande arbete inom Ringhals.

Arbetet innebär mycket frihet under ansvar varför du behöver vara självgående, noggrann och serviceinriktad. För att kunna bidra till enhetens utveckling vill vi att du är kreativ, lyhörd och positiv till förändringar. Det är även viktigt att du tycker om att arbeta i grupp och vill bidra i vårt gränsöverskridande arbete inom Ringhals.

Om verksamheten
Ringhals AB ingår i Vattenfallkoncernen och är Nordens största kraftverk. Vi har över 40 års erfarenhet av elproduktion och står nu inför nya utmaningar av olika slag som kräver säkerhetsmedvetande och nytänkande. Ringhals har ca 1 300 anställda och ligger på västkusten i Varbergs kommun, sex mil söder om Göteborg.
Vår medarbetarkultur präglas av kompetens, kunnande och positiva människor som vill dela med sig av sina kunskaper. På Ringhals arbetar vi ständigt med att utveckla vår verksamhet och vårt arbetssätt för att kunna nå de krav som kunder och omvärld ställer på oss, varför vi ser individens utveckling som en stor del av företagets framtid. Hos oss erbjuds du personlig utveckling på en arbetsplats med många möjligheter.
Läs gärna mer om verksamheten https://group.vattenfall.com/se/var-verksamhet/ringhals

Placeringsort: Ringhals

Vattenfall är en del av Sveriges kritiska infrastruktur och vår verksamhet omfattas bland annat av regler om säkerhetsskydd, nukleär icke-spridning och exportkontroll. På grund av dessa regler genomförs en kontroll av kandidaten för många av tjänsterna i vår verksamhet innan anställning sker. För de tjänster som leder till deltagande i säkerhetskänslig verksamhet eller placering i säkerhetsklass innebär denna kontroll att säkerhetsprövning genomförs i enlighet med säkerhetsskyddslagen.

Denna rekrytering hanteras av QRIOS Life Science & Engineering. Vi är ett ackrediterat konsult och rekryteringsföretag som är starkt inspirerade av dem som aldrig slutar leta efter nya lösningar. Som vi säger, QRIOS MINDS GO FURTHER.
Varmt välkommen med din ansökan redan idag!

#LI-UE1

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Utvecklingsingenjör skydd, Ringhals

Skyddsingenjör
Läs mer Mar 7
Utvecklingsingenjör skydd, Ringhals

Om tjänsten
Vill du vara med och bidra till Sveriges fossilfria elförsörjning?

Nu har du möjlighet att göra det hos oss på Ringhals. Vi arbetar tillsammans för att göra Sverige fossilfritt inom en generation. För att nå vårt mål behöver vi engagerade medarbetare som vill arbeta hos en av Sveriges största elproducenter och samtidigt bidra till ett bättre klimat på vår planet.

Vi är övertygade om att mångfald berikar, och arbetar därför kontinuerligt för jämställdhet och inkludering på vår arbetsplats. Läs gärna mer om vårt arbete inom mångfald och inkludering på vår hemsida https://careers.vattenfall.com/se/jobba-med-oss/

Är du intresserad av strålning och dess påverkan på människan, anläggningen och omgivningen samt har viljan och intresset att agera som skyddsbarriär på Ringhals? – då kanske du ska söka dig till NSR – Radiologi och operativt skydd.

Dina arbetsuppgifter i huvudsak
NSRO - operativt skydd ansvarar för att utföra, utveckla och förvalta uppgifter inom verksamhetsområdet (Skydda individ, anläggning och omgivning) för hela företaget. Som utvecklingsingenjör skydd kommer du arbeta inom området operativ skydd, vilket innefattar både strålskydd och arbetsmiljö.

Som utvecklingsingenjör är dina huvudsakliga arbetsuppgifter:
• Planering, genomförande och analyser inom verksamhetsområdet strålskydd och radiologi
• Genomföra händelse- och orsaksutredningar
• Rapportskrivning, uppdatering och granskning av instruktioner och anvisningar.
• Upprätthållande av kontaktytor, både internt och externt med såväl Strålsäkerhetsmyndigheten som övriga Kärntekniska anläggningar.
• Omvärldsbevakning och utveckling av verksamheten

Vi erbjuder ett utåtriktat och självständigt arbete som utvecklingsingenjör skydd. Du kommer att fungera som tekniskt stöd och kompetent resurs inom området för övriga organisationen. Hos oss bidrar du med nyckelkompetens inom strålskydd och radiologi i det löpande och långsiktiga arbetet under drift och avveckling.

Arbetet spänner över ett brett verksamhetsområde och innebär både praktisk och administrativt arbete. Att agera som instruktör i NSR strålskyddsutbildningar samt ingå i RIHAB ingår också i tjänsten.

Vem är du?
Vi söker dig som har högskoleingenjörsexamen eller motsvarande relevanta kunskaper inom strålskydd och radiologi och har flera års arbetslivserfarenhet inom kärnkraftindustrin. God anläggningskännedom på Ringhals är meriterande.

Arbetet innebär mycket frihet under ansvar varför du behöver vara självgående, noggrann, initiativtagande, och kommunikativ.

För att kunna bidra till enhetens utveckling vill vi att du är kreativ, lyhörd och positiv till förändringar. Det är även viktigt att du tycker om att arbeta i grupp och vill bidra i vårt gränsöverskridande arbete inom Ringhals.

Som person planerar, organiserar och prioriterar du arbetet på ett effektivt sätt. Du sätter upp och håller tidsramar. Du tar initiativ, sätter igång aktiviteter och uppnår resultat.

Om verksamheten
Ringhals AB ingår i Vattenfallkoncernen och är Nordens största kraftverk. Vi har över 40 års erfarenhet av elproduktion och står nu inför nya utmaningar av olika slag som kräver säkerhetsmedvetande och nytänkande. Ringhals ligger på västkusten i Varbergs kommun, sex mil söder om Göteborg.

Vår medarbetarkultur präglas av kompetens, kunnande och positiva människor som vill dela med sig av sina kunskaper. På Ringhals arbetar vi ständigt med att utveckla vår verksamhet och vårt arbetssätt för att kunna nå de krav som kunder och omvärld ställer på oss, varför vi ser individens utveckling som en stor del av företagets framtid. Hos oss erbjuds du personlig utveckling på en arbetsplats med många möjligheter.

Läs gärna mer om Vattenfalls verksamhet https://group.vattenfall.com/se/var-verksamhet/ringhals

Placeringsort: Ringhals

Vattenfall är en del av Sveriges kritiska infrastruktur och vår verksamhet omfattas bland annat av regler om säkerhetsskydd, nukleär icke-spridning och exportkontroll. På grund av dessa regler genomförs en kontroll av kandidaten för många av tjänsterna i vår verksamhet innan anställning sker. För de tjänster som leder till deltagande i säkerhetskänslig verksamhet eller placering i säkerhetsklass innebär denna kontroll att säkerhetsprövning genomförs i enlighet med säkerhetsskyddslagen.

Denna rekrytering hanteras av QRIOS Life Science & Engineering. Vi är ett ackrediterat konsult och rekryteringsföretag som är starkt inspirerade av dem som aldrig slutar leta efter nya lösningar. Som vi säger, QRIOS MINDS GO FURTHER.
Varmt välkommen med din ansökan redan idag!

#LI-UE1

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Laboratorieingenjör / Göteborg

Laboratorieingenjör, kemi
Läs mer Mar 28
På uppdrag av vår världsledande samarbetspartner söker vi nu en driven laboratorieingenjör som är i början av sin karriär med intresse att utveckla nya hälsofrämjande produkter. Konsultuppdraget kommer att starta omgående och vara baserad i centrala Mölndal.

Om tjänsten
I rollen som laboratorieingenjör kommer du snabbt fördjupa dina labbfärdigheter och bredda ditt professionella nätverk. Du kommer att ingå i ett framgångsrikt labbteam vars gemensamma målsättning är att utveckla nya hälsofrämjande produkter med fokus på cirkulär hållbarhet. Du uppmuntras att ta initiativ samt komma med nya idéer och förbättringsförslag med stor möjlighet till projektansvar.

Dina arbetsuppgifter i huvudsak
Dina arbetsuppgifter innefattar bland annat att:
• Planera, testa, analysera och statistiskt utvärdera olika material som utvecklas inom bolaget.
• Presentera, dokumentera och rapportera testresultat
• Upprätthålla kunskap om testmetoder för att stötta kollegor på andra avdelningar i bolaget med specifika materialanalyser
• Delta i innovationsprojekt samt arbeta i tvärfunktionella team
• Utveckla, utvärdera och validera nya laboratoriemetoder för att möta konsumenternas och företagens behov

Vem är du?
För att ha rätt förutsättningar i rollen ser vi att du har:
• Teknisk universitetsexamen (minst kandidatexamen helst i kemi, mekanisk eller textil)
• God erfarenhet av statistisk analys och analytisk förmåga är meriterande
• God kommunikations- och presentationsförmåga i såväl skriftliga rapporter som i diskussioner
• Behärskar svenska och engelska i tal och skrift

Det är mycket meriterande om du har tidigare erfarenhet av labbarbete i industrin!


Om verksamheten
QRIOS kan erbjuda flera möjligheter till dig som är ingenjör eller har en teknisk bakgrund. Våra uppdragsgivare finns inom miljö-, energi-, skogs-, fordons-, läkemedels-, livsmedels-, process- och produktionsindustrin. Oavsett om du vill arbeta på ett stort eller litet företag, inom privat eller offentlig sektor, så har vi en tjänst för dig. Vi förenar människor och teknik!

Att vara konsult hos oss ger dig många möjligheter att prova på olika branscher, företag och roller. Läs gärna mer om hur det är att vara konsult hos oss: https://www.qrios.se/om-oss. Det passar dig som vill få mycket erfarenhet under en kortare period. Om du letar efter en värld fylld av spännande möjligheter och nya kontakter kommer du gilla att vara konsult hos oss.



Varmt välkommen med din ansökan. Urval sker löpande, ansök därför redan idag genom att klicka på ansök på https://www.qrios.se.

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