Göteborg: Senior Research Scientist / Research scientist – RIA Bioscience

About the position
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.

Research Scientist position – in vitro cellular profiling
We are looking for a passionate Research Scientist to join our Mechanistic and Structural Biology department within the Discovery Sciences organization in Gothenburg, Sweden. You will apply your proven cell biology expertise to in vitro cellular assays. Routine profiling will be combined with tailored mechanism of action studies in cellular models across a multitude of different drug discovery projects. You will build a detailed understanding of the impact of treatment by multiple drug modalities, including small molecules, PROTACS and therapeutic oligonucleotides.
You will demonstrate a passion for applied science, combined with a strong emphasis on team work. You will join a team whose remit is to support our drug discovery projects globally with early DMPK assessment, SAR profiling and detailed mechanism of action data. We offer a highly rewarding scientific environment with ample learning opportunities.
You will be strongly encouraged and supported to think creatively in our dynamic environment. Here, we are free from fear of failure, free to ask the right questions and make bold decisions.

Responsibilities
What you will do:
This is a lab-based role focused on generating routine screening data and bespoke in vitro pharmacology studies in support of drug discovery projects. The work includes independent troubleshooting and timely reporting of data according to agreed timelines. All work is conducted in close dialog with project teams, specifically in support of the Cardiovascular, Renal and Metabolism as well as Respiratory & Immunology disease area organisations locally in Gothenburg.

Your profile
Essential to the role and desirable skills:

-MSc or PhD within a relevant scientific discipline or demonstrated relevant experience in the Life Science industry.
-Proven track record of cellular biology techniques and pharmacology studies.
-Compound profiling in a screening environment using microtiter plates and automation as well as experience in the design, development and validation of biological test assays for compound profiling.
-Practical knowledge of high-resolution MS for targeted or global proteomics analysis and several technology platforms such as imaging, flow cytometry and LC-MS
-Good knowledge of oral and written English is a requirement

Soft skills:
Excellent communication skills and an ability to operate effectively in a multi-disciplinary research environment.
Independent analysis and evaluation of complex data and delivery of data to agreed timelines.
First-rate decision-making skills, coupled with tenacity to see decisions through, even in situations of ambiguity.

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.

About the position
Would you like to utilise your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines.

We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in AstraZeneca’s trials all over the world. Our goal is to never miss a patient.

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.

Responsibilities
In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study.

To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills.

Your main responsibilities will include:
• Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply.
• Ensure effective communication with project teams and key partners across a global network.
• Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies.
• Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction.
• Manage the Interactive Response Technology (IRT) system to execute demand and supply planning.
• Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls.

Your profile
• Bachelor’s Degree in a scientific or supply chain subject area – equivalent experience will be considered.
• Experience within a supply chain management environment with a holistic knowledge of end-to-end supply chain activities
• Experience of demand planning and forecasting and risk identification and management
• Experience in running projects and in?uencing customer demands.
• Strong in?uencing, negotiating and problem-solving skills, across geographical and cultural boundaries
• Excellent English written and verbal communication skills.
• Proficient IT skills with an ability to adapt and operate in bespoke multiple systems.

Desirable for the role
• Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice)
• Knowledge of clinical development processes relevant to the supply of clinical materials
• Lean knowledge and understanding
• Experienced in handling Quality Events (Deviations, Change Controls, Complaints)

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.

About the position
We are now looking for a Scientist to join the In vivo Bioscience team within Research and Early Development, Respiratory & Immunology in Gothenburg, Sweden.

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. In this role, you will focus on mouse models of inflammatory bowel disease (IBD).

Responsibilities
As part of the team, you will plan, execute and analyse ex vivo samples generated from in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You will actively take part in scientific discussions to add valuable inputs in experimental design and data interpretation.

This is a mainly lab-based role where you will be involved in ongoing projects focusing on pre-clinical experiments.

What you’ll do:

• As a Scientist you will be a vital member of the in vivo community and will contribute to the development and characterization of pre-clinical models of IBD to discover novel therapeutics.
• You will contribute to the analysis of in vivo studies with a specific focus on FACS analysis.

Your profile
• At last 5 years of experience with regular FACS analysis of mouse samples (organ processing and digestion, cell staining, antibody panel set up, proficient in the use of BD FACS DIVA machines and Flowjo).
• Ability to organize, execute and interpret the results from in vivo studies according to study plans in agreement with the team leader or other colleagues.
• Experience with other in vitro methodology in addition to FACS (ELISA/MSD and/or qRT-PCR) to analyze ex vivo samples generated from in vivo studies.
• Experience of maintaining the highest standards of welfare and ethical compliance and ensuring the integrity of the 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.
• Valid education required for compliance to work with live animals in Sweden.
• Excellent English written and oral communication skills, including presentation skills.

Desirable for the role:

• Degree in immunology (master or PHD) and understanding of autoimmune diseases with a specific focus on gut immunology.
• Several years of hands-on experience with rodents including live animal handling, drug administration through different routes (i.v, i.p., p.o.), blood and organ sampling and processing (colon, small intestine, spleen, lymph nodes).
• Experience with animal models of inflammatory bowel disease (IBD) and in vivo PK/PD relationships.

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.

Vi ser ett ökat behov hos våra kunder vilket gör att vi nu söker både juniora och seniora administratörer till vår olika kunder i Göteborg.

Våra uppdragsgivare befinner sig inom olika branscher vilket gör att rollen som administratör kommer varierar beroende på bransch och kundernas behov.

Denna annons är en generell annons som inte är kopplad till en specifik tjänst.
Urval och intervjuer kommer att ske löpande så välkommen med din ansökan redan idag!

Vad blir mina arbetsuppgifter?
Som administratör sträcker sig arbetet över ett brett område. Tjänsterna innehåller både enklare och mer kvalificerade arbetsuppgifter. Arbetsuppgifterna kan därför variera och innehålla allt från rutinarbete till mer kvalificerade uppgifter såsom:

• Planera och organisera mötesdokumentation, konferens- och resebokningar
•Administration
•Reseadministration
•Posthantering
•Protokollföring
•Diarieföring
•Rapportskrivning
•Externa och interna kontakter
•Framtagande av statistik och informationssökning
•Ekonomisk administration i form av konteringar
•Växeltelefoni
•Reception

Är du den vi söker?
Vi söker dig som har erfarenhet av ett liknande arbete samt har goda administrativa kunskaper. I rollen som konsult krävs det att du snabbt kan ta dig an nya arbetssituationer och har en förmåga att uppfatta helheten.

Vi ser att du har en öppen och positiv attityd samt en god förmåga att skapa kontakter och har lätt för att komma in i nya rutiner. Du har ordet service som ledord och ett driv att vilja leverera goda prestationer. Det är viktigt att du är noggrann, strukturerad, lyhörd och flexibel, samt trivs att arbeta med varierande arbetsuppgifter.

Vidare är du initiativtagande och självständig i ditt arbete. Ett krav är att du har goda erfarenheter inom Officepaketet samt behärskar det engelska språket flytande i tal såväl som skrift.

Det är meriterande om du har erfarenhet från fordonsindustrin eller från en annan internationell miljö samt har god kännedom av affärssystemen SAP och SharePoint.
Vad kan vi erbjuda dig som konsult?
Konsultrollen passar dig som på kort tid vill skaffa dig bred erfarenhet. Vi erbjuder dig chansen att arbeta på populära arbetsplatser med välkända varumärken där du kan utveckla din kompetens och bredda ditt CV. Du kommer att trivas som konsult om du söker en värld av spännande uppdrag och nya kontaktnät. Vid din sida har du din konsultchef som agerar bollplank och stöttar dig i att lyckas på dina uppdrag.
Vi vill att du ska må bra och trivas med oss på Poolia. Därför erbjuder vi dig friskvårdsbidrag, rabatter på olika träningsanläggningar och ordnar regelbundet sociala aktiviteter. Självklart omfattas din anställning på Poolia av kollektivavtal, försäkringar, tjänstepension samt företagshälsovård.

Är du en driven redovisningsekonom med erfarenheter från affärssystemet IFS? Då kan detta vara tjänsten för dig. Renova Miljö är ett ledande miljöföretag inom avfall och återvinning och söker nu en redovisningsekonom till deras verksamhet. Uppdraget
är på heltid och sträcker sig i 6 månader med chans till förlängning. Välkommen med din ansökan redan idag!

Vad blir mina arbetsuppgifter?
Du kommer att ingår i koncernens interna ekonomifunktion där du får mycket goda utvecklingsmöjligheter. Tillsammans med ditt team är du ansvarig för både intern och extern redovisning, bokslut och rapportering gällande företagets olika verksamhetsgrenar. Du hanterar, leder och utvecklar processer för optimering av metoder samt arbetssätt gällande rapportflödet från det lokala till det gemensamma. Genom policys och riktlinjer ser du till att all finansiell rapportering och redovisning sker enligt intern standard samt god redovisningssed. Dina huvudsakliga arbetsuppgifter:

-Sammanställa månads- och årsbokslut
-Hantering av momsdeklarationer
-Löpande bokföring och redovisning
-Rapportera till ledning och styrelse

Du kommer arbeta i centrala Göteborg under kontorstider med möjlighet till flex.

Vad krävs för denna spännande tjänst?
Som person är du en lagspelare med ett starkt driv att nå uppsatta mål. I ditt dagliga arbete har du nytta av din analytiska förmåga och ditt helhetsperspektiv när du med effektivitet löser de problem som kan uppstå. Vidare är du leveranssäker, självständig och har förmågan att prioritera din tid på ett effektivt sätt för att möta deadlines. Slutligen är du initiativtagande, flexibel och kan arbeta proaktivt i en föränderlig miljö. I övrigt ser vi att du har;

-Universitets- eller högskoleutbildning inom ekonomi eller finans.
-Du är trygg i rollen som redovisningsekonom och har några års arbetslivserfarenhet
inom området.
-God systemvana främst i Excel och Office MS.
-Behärskar svenska och engelska i tal och skrift.
-Erfarenhet av att arbeta i affärssystemet IFS.
Vilka är Renova?
Som Västsveriges ledande aktör inom avfall och återvinning har vi en viktig roll att fylla. Vi bidrar till kretsloppet genom att återvinna avfall till energi och nya råvaror. Genom att aktivt satsa på forskning och utveckling tar vi också ansvar för framtiden.

Allt vi gör på Renova bidrar till ett mer hållbart samhälle. Vårt uppdrag är att skapa affärsmässig samhällsnytta genom att ta ett långsiktigt ansvar för miljöriktig och kostnadseffektiv avfallshantering och återvinning.
Vad kan vi erbjuda dig som konsult?
Konsultrollen passar dig som på kort tid vill skaffa dig bred erfarenhet. Vi erbjuder dig chansen att arbeta på populära arbetsplatser med välkända varumärken där du kan utveckla din kompetens och bredda ditt CV. Du kommer att trivas som konsult om du söker en värld av spännande uppdrag och nya kontaktnät. Vid din sida har du din konsultchef som agerar bollplank och stöttar dig i att lyckas på dina uppdrag. Vi vill att du ska må bra och trivas med oss på Poolia. Därför erbjuder vi dig friskvårdsbidrag, rabatter på olika träningsanläggningar och ordnar regelbundet sociala aktiviteter. Självklart omfattas din anställning på Poolia av kollektivavtal, försäkringar, tjänstepension samt företagshälsovård.

Are you a service professional with a true passion in delivering the best results for customers? Do you have experience of administrative work and a technical interest? If yes, you might be just the one we are looking for. We at Poolia have a great opportunity for you to work as Back Office Support for an international company in Gothenburg. This is a part-time position (50%) and we would like you to be availabe in middle of May. Keep reading and send your application today, interviews are held continuously and the position might be filled before the end date!

About the role:
You will have variation of administrative tasks and you will have daily contact with both customers and suppliers. You will work weekdays where you will be able to work both full and half days in the form of mornings. Perfect for a student or for you who are looking for a part-time postion.

Responsibilites:

-Working with customer support cases, over email and Skype.
-Order and offer handling and payment questions.
-Developing and maintaining working relationships with appropriate individuals or groups globally to ensure success in the daily activities.
-Be in charge of reclamations, investigations and other reports.

Who are we looking for?
In order to succeed in the role, we believe that you have experience of working with customers. You as a person are a team player who is used to working at a high pace and has no problems switching up a level when needed. We see that you are organised, efficient and not afraid to take your own initiatives. We also like you too;

-Have experience of administrative or support work, preferably with a focus on technical issues.
-Very good computer skills, mainly in MS Office and Excel.
-Fluent English is required, both verbally and in writing.
-You have a technical interest.

Russian language and experience of working in M3 system can be an advantage.
How to apply?
It's easy! Just push the apply button and you're on your way. Selection and interviews will be helt continuously.