Göteborg: Distribution Operator

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Publicerad: 2024-05-15 // Varaktighet: Heltid

We now 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 operational role within Distribution one of Drug Product Deliveries three operational skill areas, Material Management, Pack Label and Distribution. We work in an 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
- 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
The role holder will contribute to the DPD organization applying their expertise in the complex and regulated GMP environment. The work is focused operational within Distribution. 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.
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.

Your profile
Essential requirements:
-BSc/MSc in chemistry/pharmacy/engineering or equivalent experience. Preferably 2 years experience within pharmaceutical development
-Understanding the disciplines in Drug Product Delivery, Supply Chain and Pharmaceutical development in order to contribute to an effective Supply Chain organization
-Understanding of principles, applications and management of SHE and GMP in an R&D environment
-Demonstrated ability to work with teams in a culturally diverse, complex and changing environment most internally but to some extent externally
-Good written and verbal English communication and understanding

Soft skills:
As a person, you should have a curious and innovative mindset with problem solving ability, resolving issues with minimal guidance. The perfect candidate should show interest in working operationally to learn and quickly adapt to the new tasks with a willingness to develop within this role.

About the organisation
This is a consultant assignement for one year util June 2025 at AstraZeneca Göteborg.
During this time you will be hired by QRIOS.

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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Andra jobb i Göteborg som Forskare, farmakologi

Nedan visas andra jobb i Göteborg som Forskare, farmakologi.

Scientist in the Microphysiological Systems

Läs mer Jan 28
About the position
Do you have strong experience in cell culture and you would like to apply your expertise in a company that is accelerating innovative science and turn ideas into life changing medicines? Join our Microphysiological systems (MPS) team to discover future preclinical models that can support development of new medications for Cardiovascular, Renal and Metabolic diseases!

At AstraZeneca, we are harnessing advanced cell models, microfluidic chip technologies, multi-omics screens, and mathematical modelling to help us achieve the next wave of breakthroughs – here we do things that have never been done before. Are you excited to contribute, then you might be the person we are looking for!

This role will be based in the MPS team at the Early Cardiovascular, Renal and Metabolism (CVRM) department in our dynamic R&D site in Gothenburg, Sweden. The MPS team establishes and applies state-of-the-art MPS platforms to support the CVRM portfolio with emerging therapeutic area needs and new drug modalities. Our mission is to improve translatability from in vitro models to humans and accelerate drug discovery and development.

Responsibilities
You will execute and provide input into the practical delivery of MPS studies and support the development, characterization, and optimization of new models.

Responsibilities include:

• Take part in the design, conduct, interpretation and reporting of studies with advanced cell models and MPS.
• Carry out various downstream analyses from the cell culture samples with versatile in-vitro analytical methods such as, but not limited to, ELISA’s, qPCR, staining and imaging.
• Join further model development activities to support drug projects with MPS data for resolving mechanisms of action, target identification, and candidate drug evaluation.
• Effectively communicate and collaborate across the Early CVRM and with the key stakeholders in other functions.

Your profile
Essential for the role:

• Master’s degree + 2 years of relevant experience.
• Background in Pharmacy, Biology, Biotechnology, Biochemistry, Medical Biosciences, Bioengineering or similar
• Strong hands-on cell culture experience
• Experience with primary cells or hPSCs
• Versatile in-vitro analytical methods (e.g., qPCR, staining and high-content imaging, plate-based assays e.g., ELISAs)
• Independent study design, laboratory work, and data analysis
• Data visualization and statistical analysis
• Excellent interpersonal skills and excellent communication skills in English, both verbal and in writing
• Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery

Desired for the role:

• Experience in 3D cell culture, i.e., spheroids, organoids, or multicellular co-cultures
• Experience with one or more of cell models for liver, kidney, cardiac, pancreas, or adipose tissue
• Experience in culturing immune cells
• Handling microfluidic chips
• RNA-Seq and proteomics
• Workflow automation e.g. robotic liquid handling
• Experience from the pharmaceutical industry

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg for 1 year, starting in April 2025.
During this time you will be hired by QRIOS.

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.

Ansök nu

Flow cytometry Sr Scientist in the Microphysiological Systems

Läs mer Jan 28
Do you have experience in flow cytometry and versatile knowledge in cell culture, and are you eager to apply your expertise in a company that accelerates innovative science to turn ideas into life-changing medicines? Join our Microphysiological Systems (MPS) team and contribute to the discovery of future preclinical models that support the development of new medications for Cardiovascular, Renal, and Metabolic (CVRM) diseases!

About the position
At AstraZeneca, we are harnessing advanced cell models, microfluidic chip technologies, multi-omics screens, flow cytometry, and mathematical modelling to achieve the next wave of breakthroughs – here we do things that have never been done before. Are you excited to contribute? Then you might be the person we are looking for!

This role is based in the MPS team at the Early CVRM department in our dynamic R&D site in Gothenburg, Sweden. The MPS team establishes and applies state-of-the-art MPS platforms to support the CVRM portfolio with emerging therapeutic area needs and new drug modalities. Our mission is to improve translatability from in vitro models to humans and accelerate drug discovery and development.

Responsibilities
You will execute and provide input into the practical delivery of MPS studies while also serving as a flow cytometry (FACS) scientist. You will support the development, characterisation, and optimisation of advanced cell models and flow cytometry-based assays. We’ll look to you as an expert in cell and molecular biology techniques, and you will independently carry out various downstream in-vitro analytical methods.

Responsibilities include:

• Develop and execute flow cytometry-based assays for cell characterisation and functional analysis including panel design.
• Take part in the design, conduct, interpretation, and reporting of studies with advanced cell models and MPS.
• Carry out various downstream analyses from cell culture samples with versatile in-vitro analytical methods such as, but not limited to, ELISA, qPCR, staining, and imaging.
• Join further model development activities to support drug projects with MPS and flow cytometry data for resolving mechanisms of action, target identification, and candidate drug evaluation.
• Effectively communicate and collaborate across the Early CVRM department and with key stakeholders in other functions.

Your profile
Essential for the role:

• Master’s degree + 4 years of relevant experience.
• Background in Pharmacy, Biology, Biotechnology, Biochemistry, Medical Biosciences, Bioengineering, or similar.
• Proficiency in flow cytometry, including assay development, troubleshooting, and data interpretation.
• Strong hands-on cell culture experience.
• Versatile in-vitro analytical methods (e.g., qPCR, staining and high-content imaging, plate-based assays such as ELISAs).
• Independent study design, laboratory work, and data analysis.
• Data visualization and statistical analysis.
• Strong interpersonal and communication skills in English, both verbal and written.
• Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery.

Desired for the role:

• Experience in 3D cell culture, i.e., spheroids, organoids, or multicellular co-cultures.
• Experience with one or more of the following cell models: liver, kidney, cardiac, pancreas, or adipose tissue.
• Experience in culturing immune cells.
• Handling microfluidic chips.
• Workflow automation, e.g., robotic liquid handling.
• Experience from the pharmaceutical industry.

About the organisation
This is a consultant assignment at AstraZeneca in Göteborg for 1 year, starting in April 2025.
During this time you will be hired by QRIOS.

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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Product Director, Site & Sponsor Products

Läs mer Feb 7
Nytt
Evinova enables global life sciences to accelerate better health outcomes, by creating digital health solutions for clinical research. We are a separate business within the AstraZeneca group.

Our highly configurable SaaS solutions are used by patients, research sites, sponsors, and CROs throughout the clinical study lifecycle. As our business scales, we need the extend the team and adopt our organization to keep focus on a number of key areas. Site & Sponsor Products is a key part of our service and is a critical and strategic area for our vision to transform clinical trials, enhance participant experience and improve patient health outcome. This area includes our Unified Trial Solution (UTS) as well as specialized AI driven products to support specific Site/Sponsor processes (AIDA).

We are now hiring a Director Site & Sponsor Products to join our team. In this role, you will lead a team of Product specialists together with subject matter experts focused on Products and services for site and sponsor staff before, during and after a clinical trial. The team will be responsible for design and development of products to transform the experience for site & sponsor staff while enabling new novel designs of clinical trials to accelerate delivery and improve quality while satisfying regulatory and legal requirements and guidelines. Together with other specialist across design, engineering and customer delivery the team will define and develop requirements for future product(s) and deliver them in an efficient way and align with the Head of UTS Core for overall Product alignment.

You, and your team, will work closely with Clinical Operations specialists internally or externally to define opportunities and improvements in the set-up, management, delivery and close-out of Clinical trials. Your team will be responsible for improving metrics about speed of delivery, user experience and quality in the clinical trial execution as supported by our products. You will also work closely with the Digital Strategy Directors community to understand and influence digital disease area strategies to make full use of Product opportunities and services.

This is a highly strategic role where you will need to balance the "big picture" with a deep understanding of the technical and operational details. You will work with other part of the company to secure that the product fits in an efficient and customer focused end-to-end service to make participation in clinical trials as easy as possible while securing the integrity of all data collected. Fostering a learning organization and sharing knowledge will also be a critical part of the responsibilities.

Essential Requirements

* Life Sciences degree or equivalent experience
* Extensive Product Management skills, +5 years, in similar product areas
* 5 or more years' experience from relevant roles in delivery of clinical trials and deep knowledge of DPS components and their utilization in clinical trials.
* Understanding of the drug development process, and the different sources of information that will support, inform and assist in Trial Design and execution.
* Knowledge of GCP, 21 CFR part 11, relevant guidelines ISPOR, ISOQOL, FDA, EMA
* Proven track record of teamwork in a cross functional setting with internal as well as external partners
* Ability to challenge the status quo, lead through a vision, take ownership and hold self and others accountable.
* Well-developed Senior Stakeholder management skill with together with proven problem-solving, collaboration and interpersonal leadership skills
* Effective problem and conflict solving skills.
* Excellent written and verbal communication skills, with the ability to deal with ambiguity and create clarity.
* Great leadership skills and experience in developing people.
* Ability to work collaboratively in a cross functional setting with internal as well as external partners.
* Passion for Customers, representing the needs of multiple customers in decision making.
* Experience of Deployment of scaled products

Desirable

* Thrives in a fast-paced work environment, comfortable with complexity and uncertainty at times, lots of humour, dedication to deliver outcomes and motivated by the opportunity to rethink our approach to healthcare.
* Comfort and skills operating in a heavily matrixed organizations with excellent skills and intuition to manage the needs of various partners.
* Ability to manage and influence strategically and persuade tactfully, to acquire desired outcomes while maintaining effective, positive, organizational relationships.

* Comprehensive understanding of dynamics affecting the pharmaceutical industry and needs for transformation.

* Ability to work globally including international travel.

Why Evinova?
Evinova draws on AstraZeneca's deep experience developing novel therapeutics, informed by insights from thousands of patients and clinical researchers. Together, we can accelerate the delivery of life-changing medicines, improve the design and delivery of clinical trials for better patient experiences and outcomes, and think more holistically about patient care before, during, and after treatment. We know that regulators, healthcare professionals, and care teams at clinical trial sites do not want a fragmented approach. They do not want a future where every pharmaceutical company provides its own, different digital solutions. They want solutions that work across the sector, simplify their workload, and benefit patients broadly. By bringing our solutions to the wider healthcare community, we can help build more unified approaches to how we all develop and deploy digital technologies, better serving our teams, physicians, and ultimately patients. Evinova represents a unique opportunity to deliver meaningful outcomes with digital and AI to serve the wider healthcare community and create new standards for the sector.



Location
The office is based in Gothenburg. We have an on-site commitment of three days a week.

Welcome to apply!

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Senior Director BioPharma Project Toxicology Team

Läs mer Feb 3
Are you ready to lead a team that makes a significant impact on the development of life-changing medicines? AstraZeneca is looking to recruit a dedicated and experienced Project Toxicologist at the Senior Director career level to provide non-clinical toxicology leadership to our team of project toxicologists supporting our exciting BioPharma portfolio, supporting cardiovascular, renal, metabolic, and respiratory indications. The position can be based at one of our vibrant strategic R&D sites in Gothenburg (Sweden), Gaithersburg (US), Cambridge (UK) or Barcelona (Spain).



As an empowered Project Toxicologist in BioPharma Safety, you will be responsible for globally supporting the people, portfolio, and productivity goals of the BioPharma Safety project toxicology team. This position requires an experienced toxicologist with a keen understanding of operational systems, processes and portfolio resourcing requirements to ensure efficient and sustainable delivery of pipeline and marketed product non-clinical toxicology. Your inclusive leadership will foster talent growth, adapt creativity, and encourage a supportive environment where each colleague achieves their full potential. This role will report to the head of BioPharma Safety and will be a member of the BioPharma Safety department leadership team.





Your main accountabilities will be:

*

Lead an enthusiastic BioPharma Safety Project Toxicology team (approximately 10 direct reports), ensuring that they provide optimal toxicology support to the BioPharma portfolio, including candidate selection, first-time in human-enabling, early and late stage development, and marketing activities
*

Act as project toxicologist leading the nonclinical safety aspects of assigned early and late stage BioPharma projects, including high profile development projects / products and externalization, and in-licensing evaluation activities
*

Guide and coach project toxicologists on both technical and operational toxicology aspects
*

Performance management of the project toxicology team, setting goals and objectives, providing feed forward coaching, appropriate development opportunities and effective succession planning
*

Proactive planning and resource forecasting as line manager to ensure effective and sustainable portfolio support
*

Partner with Strategic Toxicology Leads, Discovery Safety leaders, Safety Innovation and Regulatory Toxicology Safety Pharmacology, Pathology, Operations departments and external partners to secure peer input and resource vs safety work across the portfolio
*

Build networks with other teams, external partners and external stakeholders to learn about new developments, leverage opportunities and share best practices
*

As a BioPharma Safety Leadership Team member, you will identify, set, and deliver on overall department objectives and talent development whilst upholding a diverse, inclusive and safe environment for staff





Essential Skills/Experience

*

A PhD education (or equivalent) in Toxicology or a related life-science subject, with extensive experience working as a Toxicologist within a pharmaceutical project environment
*

Extensive knowledge and experience of delivering in all development phases of small molecule and/or biologics drug development from early discovery to marketing; from a nonclinical perspective but also with a good understanding of key partners such as Clinical, pharmacovigilance, Regulatory, CMC functions and contract research organizations.
*

Significant experience in providing expert design and interpretation of toxicology programs supporting clinical development and marketing of biopharma registration of drugs products.
*

Specialist knowledge and extensive experience of the cardiovascular, renal, metabolism, and respiratory therapy areas
*

Excellent influencing and project leadership skills; ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues and deliver business impact
*

Ability to operate with sensitivity and flexibility within an ever-evolving organizational matrix of project and line management, both functionally and across the business
*

Willingness to challenge conventional thinking and implement creative ideas balanced with a high regard and understanding for the regulatory framework in which AstraZeneca operates



At AstraZeneca, we believe in the power of unconventional collaboration-when diverse minds come together, innovation is infinite, resulting in life-changing advancements. While we work in the office at least three days a week, we embrace flexible working that respects personal needs and drives productivity.



Be a part of our passion for scientific innovation and make a tangible impact worldwide. Our digital, data science, and AI applications accelerate research, turning lab achievements into milestone global change. Embrace our inclusive culture and amplify your transformative contributions.





So, what's next?

We can't wait to learn more about you! Please submit your application (resume and cover letter) by 23rd February 2025.

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Separation Scientist

Läs mer Feb 3
Do you have hands-on experience with the purification of small molecules? Are you interested to further push the boundaries of automated analytical chemistry and separation sciences at a company where we are committed to lifelong learning, growth and development? Welcome to AstraZeneca!

We are seeking a specialized separation scientist that will play an important part in our iLAB team, focusing on the analysis and purification of chemical libraries. You’ll have the opportunity to drive and extend the high-throughput purification capabilities within a pioneering automation platform at AstraZeneca in Gothenburg and directly impact drug discovery projects across various therapeutic areas.

About the position
As Separation Scientist, you will be part of a team of highly motivated scientists contributing to analysis, preparative separation, and characterisation of small molecule chemical libraries. In this laboratory-based position, you will be specifically responsible for ensuring the delivery of automated analytical and preparative chromatography solutions to drive the delivery of pure compounds to the different projects across our therapy areas within AstraZeneca. You will get the opportunity to work with state-of-the-art chromatographic equipment and liquid handlers.

You will be expected to have effective levels of communication and scientific drive, coordinating effectively with the other members of the analytical and synthesis teams to drive sample progression.
Experience and technical knowledge of chromatographic separations within a drug discovery environment would be an advantage.

Responsibilities
Responsibilities for the role:

• Provide hands-on separation science support to drug discovery chemistry using state-of-the art chromatographic instrumentation
• Deliver automated analysis and purification of novel compounds using Liquid chromatography–mass spectrometry (LC–MS) and High-performance liquid chromatography (HPLC)
• Ensure reliability, performance and data quality of analytical instrumentation and automation platforms
• Work within the team to suggest process and infrastructure improvements
• Contribute to a vibrant and entrepreneurial organization focused on innovation & project delivery; collaborating closely with scientists across the discovery organization

Your profile
You’re a separation scientist with a track record of applying innovative analytical chemistry solutions. You also have:

• BSc/MSc in Chemistry or Analytical Chemistry
• Good knowledge of analytical and/or preparative chromatographic techniques (HPLC, HPLC-MS) including method development and instrument troubleshooting
• Lab-based experience using analytical chemistry and/or automation techniques
• Detailed understanding of the use of analytical techniques to solve complex scientific questions
• Ability to work in multidisciplinary team / project / function
• Excellent communication skills
• First-rate time management skills, forward planning and delivery focus, leading to good team working and a high level of self and team delivery

Desirable in the role:

• Experience from working with liquid handlers
• Experience with LC software (MassHunter, Chemstation, Masslynx, Virscidian, etc...).
• Knowledge of pharmaceutical drug discovery
• Proficiency with other analytical techniques such as NMR, IR & MS.
• Basic knowledge of synthetic chemistry.

About the organisation
This is a consultant assignement for six months at AstraZeneca in Gothenburg. Start day in March 2025.
During this time you will be hired by QRIOS.

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.

Ansök nu

Andra jobb i Göteborg från QRIOS Minds AB

Nedan visas andra jobb i Göteborg från QRIOS Minds AB .

Engagerad geotekniker till SGI

Geotekniker
Läs mer Sep 25
Om arbetsplatsen
Statens geotekniska institut (SGI) är en expertmyndighet som arbetar för ett säkert, effektivt och hållbart byggande och ett hållbart användande av mark och naturresurser. I våra uppgifter ingår att förebygga jordskred, ras och stranderosion. SGI arbetar också med att ta fram nya metoder för att sanera förorenade områden. SGI tillhör Klimat- och näringslivsdepartementet och har totalt cirka 100 medarbetare. Huvudkontoret ligger i Linköping och kontor finns i Stockholm, Göteborg och Malmö.
Göta älvdalen är Sveriges mest skredbenägna region och samtidigt det område som bedöms påverkas mest av klimatförändringen framöver. Framtida skred skulle påverka både samhällsviktiga funktioner, riksintressen, Natura2000-områden och inte minst många som bor i Göta älvdalen.
Som geotekniker i sekretariatet för Göta älv får du möjlighet att minska riskerna i denna region, du kan göra skillnad, som är till nytta för hela samhället!
Arbetsuppgifter
Det är ett välfinansierat regeringsuppdrag som möjliggör att SGI kan arbeta enligt nya utredningsmetoder med projekt från behovsanalys och fram till färdig åtgärd, optimerad enligt den senaste kunskapen. Här blir du del av en engagerad och prestigelös projektgrupp som drivs av att förbättra förutsättningarna för de som bor och verkar längs Göta älv och samtidigt fördjupa sin kunskap inom geotekniska frågeställningar.
Du kommer att leda stabilitetsutredningar samt stötta våra kommuner i deras projektering och under åtgärdsfasen med stöd från kompetenta kollegor. Arbetet innebär många kontakter, både internt och externt. Hos oss får du arbeta med helheten, Göta älv från Vänersborg till Göteborg är ett stort projekt. Sekretariatet har tillgång till en stor mängd undersökningsresultat. Såväl geotekniska beräkningsverktyg som GIS-program används i hög grad. I arbetet ingår att vara en del av SGI:s beredskapsorganisation som geotekniskt stöd till framför allt räddningstjänsten i händelse av eller vid tidiga indikationer på ras eller skred.
Kvalifikationer
Tjänsten kräver universitets- eller högskoleutbildning: civilingenjör (exempelvis väg och vatten eller samhällsbyggnad) eller liknande utbildning som av arbetsgivaren bedöms vara lämplig för tjänsten. För arbetet krävs goda geotekniska kunskaper, särskilt inom området släntstabilitet. Vi vill att du har erfarenhet av geotekniskt utredningsarbete samt projektering.

Vi löser våra uppdrag tillsammans, vilket innebär att du bör tycka om att jobba i grupp/team och att dela med dig av erfarenheter. Du ska kunna uttrycka dig väl i tal och skrift på svenska. Du har mycket god datavana och arbetar väl i Microsoft- Officepaket.
Vid urvalet kommer det att läggas stor vikt vid din personliga lämplighet. För att kunna arbeta hos oss ska du dela statens gemensamma värdegrund, http://www.sgi.se/sv/om-sgi/sa-arbetar-vi/vardegrund-och-kompass/
Vi erbjuder
Vi erbjuder dig ett samhällsviktigt uppdrag, spännande och utvecklande arbetsuppgifter med generös syn på kompetensutveckling samt en trevlig arbetsplats med medarbetare i fokus med stort engagemang och arbetsglädje. Vi har generöst med semesterdagar, möjlighet att till viss del arbeta på distans, individuell lön, flexibel arbetstid, friskvårdsbidrag, m.m.
Kontakt
Kontaktpersoner: Per Bolin, Chef för Delegationen för Göta älv, Telefon 031- 7496595, Fackliga företrädare för Saco: Martin Holmén Telefon 013 201815 ellerAdnan Drobic Telefon 031-7786572. För ST Eva Albin Telefon 013-20 18 29 eller Oskar Alm Telefon 013-201825
Övrigt
Andra placeringsorter än Göteborg kan eventuellt diskuteras. Tjänsten är en tillsvidareanställning, men provanställning kan komma i fråga. Tillträde snarast enligt överenskommelse.
Varmt välkommen att ansöka via sgi.se

Ansök nu

Geotekniker till Linköping eller Göteborgskontoret

Geotekniker
Läs mer Sep 4
Ansök via sgi.se
Om arbetsplatsen
Statens geotekniska institut (SGI) är en expertmyndighet som arbetar för ett säkert, effektivt och hållbart byggande och ett hållbart användande av mark och naturresurser. I våra uppgifter ingår att förebygga jordskred, ras och stranderosion. SGI arbetar också med att ta fram nya metoder för att sanera förorenade områden. SGI tillhör Klimat- och näringslivsdepartementet och har totalt cirka 100 medarbetare. Huvudkontoret ligger i Linköping och kontor finns i Stockholm, Göteborg och Malmö.
Arbetsuppgifter
Dina huvudsakliga arbetsuppgifter består i att ge stöd till kommuner, länsstyrelser och myndigheter avseende geoteknik i plan- och byggprocessen. Du kommer även att arbeta med kunskapsförmedling och utveckling inom geoteknikområdet.

Du kommer att ingå i SGI:s Planenhet som bland annat handlägger ärenden avseende detalj- och översiktsplaner, planläggning av infrastruktur och ärenden från mark- och miljödomstol. I tjänsten ingår även att utveckla vår verksamhet och delta i myndighetsövergripande samarbeten. Detta leder till många externa kontakter med främst myndigheter och kommuner. Arbetet innebär, förutom att leda egna uppdrag, även att medverka i andras uppdrag inom SGI:s verksamhet.

Tjänsten innefattar även medverkan i vår verksamhet med kunskapsförmedling, exempelvis kurser, seminarier och föredrag. Den som anställs kommer att ingå i SGI:s beredskapsorganisation som geotekniskt stöd till framförallt räddningstjänsten när ras eller skred inträffat eller kan befaras (TiB tjänsteman i beredskap).
Kvalifikationer
Vi söker dig med civilingenjörsexamen från Väg- och vattenbyggnadsprogrammet (Samhällsbyggnadsteknik) vid teknisk högskola eller motsvarande kompetens som arbetsgivaren bedömer likvärdig. Du bör även ha erfarenhet inom geotekniskt utrednings- eller granskningsarbete.

För tjänsten behövs goda kunskaper inom släntstabilitet och grundläggningsteknik samt geotekniskt utrednings- och projekteringsarbete. Arbetslivserfarenhet av geotekniskt arbete i planprocessen och relaterad kunskap om Plan- och bygglagen samt arbete hos annan myndighet är meriterande.

Vi vill att du ska ha intresse för samhällets och geoteknikbranschens behov av utveckling. Du ska kunna uttrycka dig väl i tal och skrift på svenska. Det är viktigt att du finner glädje i externa kontakter, uppskattar samarbete och kan inspireras av vårt samhällsuppdrag.
Vid urvalet kommer stor vikt att läggas vid din personliga lämplighet. För att kunna arbeta hos oss ska du dela statens gemensamma värdegrund, http://www.sgi.se/sv/om-sgi/sa-arbetar-vi/vardegrund-och-kompass/
Kontaktpersoner
Helene Kennedy, Avdelningschef, Telefon 031 749 65 80, Maria Kristensson, Enhetschef 031-749 6585. Fackliga företrädare:Martin Holmén,SACO 013 201815 , Eva Albin, ST Telefon 013-20 18 29
Om SGI
Statens geotekniska institut (SGI) är en expertmyndighet som arbetar för ett säkert, effektivt och hållbart byggande och ett hållbart användande av mark och naturresurser. I våra uppgifter ingår att förebygga skred, ras och erosion. SGI arbetar också med att ta fram nya metoder för att sanera förorenade områden. SGI tillhör Klimat- och näringslivsdepartementet och har totalt cirka 100 medarbetare. Huvudkontoret ligger i Linköping och kontor finns även i Stockholm, Göteborg och Malmö.

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Quality Assurance Advisor

Forskare, farmakologi
Läs mer Sep 2
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 and an eye for details 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
Responsible for quality release of manufactured Drug Product, Investigational Medicinal Product for clinical trials
Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects related to drug product
Providing quality advice and approval of documentation related to equipments, facilities, IT systems and instruments e.g. maintenance, calibration, validation and change control
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
Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working

Responsibilities
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.

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
Requirements:
• Degree in pharmacy or engineering (specializing in Pharmaceuticals)
• 2-3 years’ experience of working within a pharmaceutical GMP environment.
• Understanding of Quality Systems and GMP and related activities to Investigational Medicinal Product (IMP).
• Experience of documentation, deviations, changes, and other quality and compliance
decisions in the development projects.
• Experience preferably within a pharmaceutical manufacturing organization is desirable
• Understanding of Project Management processes is desirable
• Fluent in written and spoken English.

Softskills/personal skills:

• 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.
• Comprehensive understanding of the pharmaceutical/drug development process.
• Good communicator with experience of interacting effectively across interfaces.

About the organisation
This is a consultant assignement for 12 months at AstraZeneca Göteborg. During this time you will be hired by QRIOS.

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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Projektledare större batterilager till Soltech Göteborg

Projektledare, bygg och anläggning
Läs mer Aug 27
Vi på Soltech Energy Solutions är en samhällsbyggare som driver den gröna omställningen av energisystemet med solenergi som plattform. Detta gör vi nationellt genom storskaliga nätanslutna markbaserade solcellsanläggningar, systemlösningar för energilager och s.k. hybridanläggningar som avlastar elnätet och bidrar till att lösa energi- och effektutmaningen. Vi är ett helägt dotterbolag inom Soltech-koncernen, en av de största spelarna på den svenska solenergimarknaden, och en trygg partner som med över 30 års erfarenhet i branschen vet hur man skapar hållbara, lönsamma och högkvalitativa energilösningar. Vi söker nu en erfaren projektledare för Business Unit ESS (Energy Storage Solutions), en fristående resultatenhet som arbetar med våra systemlösningar för storskalig energilagring.
Om tjänsten
Du är en drivande kraft i fortsatt utveckling och satsning på energilager och bidrar till vår gröna vision. Som den med det övergripande projektansvaret för EPC ESS-projekt kommer du att leda och fördela arbetet inom tilldelade projekt så att tjänsten levereras med rätt kvalitet, i rätt tid och inom projektbudget för att säkerställa en hög leveranssäkerhet. Du ser till så att projektet har nödvändiga resurser och att medarbetarna har nödvändig utbildning, och du upphandlar och avropar material och tjänster till projekten. Du leder arbetet på siten och är arbetsmiljö-, miljö- och kvalitetsansvarig för projektet under EPC-tiden. Vidare är du bolagets ansikte utåt och därmed dess representant för att bygga långsiktiga och förtroendefulla relationer med kunder och externa partners.?Du överlämnar färdigställt projekt till eftermarknad och service för att säkra dess kontinuerliga förvaltning enligt kontrakt med kund. Du ingår i ett välmående och växande team som idag består av 11 medarbetare, och utgår från Stockholm/Göteborg/Jönköping. Resor i Sverige förekommer, varför du behöver ha ett svenskt B-körkort.
Vem är du?
För att passa i rollen tror vi att du har ett antal års erfarenhet som projektledare, gärna från större entreprenader inom bygg/mark/anläggning/infrastruktur/högspänningsel och liknande. Du har erfarenhet av mark-och entreprenadupphandlingar; kan de olika entreprenadformerna och förstår juridiken kring dessa liksom vikten av att ha en fungerande tidplan och att ha olika risker (som viten) under kontroll. Vi tror också att du har en högskoleingenjörs/civilingenjörsexamen inom bygg- eller maskininteknik, energi eller relaterat område - alternativt har förvärvat dina tekniska kunskaper på annat sätt. Det är bra om du är utbildad och certifierad inom en vedertagen projektmodell såsom PMI, och har du erfarenhet av batterilager, kravställningsarbete samt goda kunskaper inom entreprenadjuridik och upphandling baserat på ABT06, Ab04, AB-U eller liknande så blir ingen gladare än vi. Du får gärna ha arbetat med projektledning för bygg- och EPC-projekt samt ha erfarenhet av byggpraxis, planering, kontrakthantering, miljö- och säkerhetskrav etc. Du är en god kommunikatör och van att hantera kunder, investerare och beställare, samt brinner för och har god erfarenhet av att knyta och bibehålla stabila kundrelationer över tid. Med stort engagemang och ett systematiskt arbetssätt kombinerat med en förmåga att kritiskt granska uppgifter och på ett analytiskt vis dra slutsatser hur de skall tolkas, är du pådrivande i projekt och mån om att leverera kvalitet inom uppsatta tidsramar. Som person drivs av att åstadkomma förändring, du trivs med ett högt tempo och har ett intresse för hållbarhetsfrågor och förnybar energi. Du är en stabil, strukturerad och uthållig ledare som värdesätter samarbete och har fokus på långsiktiga mål.
Om verksamheten
Vi har både ambition och potential att vara ledande på den nordiska solenergimarknaden samt att vara bäst på att utveckla och sälja avancerade produkter och tjänster till många olika typer kunder inom fastighets, bygg- och energibranschen. Soltech Energy Solutions arbetar med större solcellsanläggningar på tak, solcellsparker, batteriparker och hybridparker. Vi vet att det är ett lagarbete och hur viktigt ett gott samarbete är både för att kunna ge våra kunder bästa möjliga lösningar och service, men också för att vi skall ha roligt på jobbet!
Soltech Energy Solutions är ett teknikdrivet tjänstemannaföretag bestående av duktiga ingenjörer, projektörer, projektledare, säljare m.m. och finns idag på orterna Stockholm, Jönköping, Göteborg, Falkenberg, Helsingborg och Malmö. För mer information: https://soltechenergysolutions.se/

Urval och intervjuer sker löpande så sök redan idag!
Varmt välkommen med din ansökan!
#LI-DW1

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Labingenjör - hälsobolag

Laboratorieingenjör, kemi
Läs mer Sep 18
På uppdrag av vår världsledande samarbetspartner söker vi nu en driven laboratorieingenjör med intresse att utveckla nya hälsofrämjande produkter. Konsultuppdraget kommer att starta omgående och vara baserad i Göteborg.
Uppdragslängden är 6 månader.

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.

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/material 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
Detta är ett konsultuppdrag hos kund i 6 månader till att börja med. Under tiden är du anställd hos oss på QRIOS.
QRIOS kan erbjuda flera möjligheter till dig som är ingenjör eller har en teknisk bakgrund. Våra uppdragsgivare finns inom olika branscher där du får möjlighet att påverka och utvecklas i din roll.


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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Research Scientist Biosamples

Forskare, farmakologi
Läs mer Aug 26
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
As a Biobank Research Scientist you will be expected to:
-Work as part of the team rotating between the following typical tasks
-Receive and register incoming HBS
-Process requests for HBS to customers, including using automated liquid handler
-Manage customer orders using specialized informatics systems as well as databases
-Respond to customer queries via mail or telephone
-Partner with Biobank groups globally as well as internal and external customers
-Work closely with other groups in the organization
-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.

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.

Your profile
• University degree in a Bioscience discipline and previous experience of laboratory work handling biological samples.
• Previous knowledge and experience (1 year) of biobanking is highly desirable.
• Experience of working with various IT solutions, including extensive knowledge of Excel, LIMS systems and database usage, is also a clear advantage.
• Experience of automated liquid handling is advantageous.
• Good analytical and problem-solving skills involving large and complex datasets is desirable.
• Excellent English, both spoken and written

• Ability to plan, perform and evaluate experiments to investigate improvement possibilities in a process.
• Knowledge of the regulatory framework of biological samples.
• 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.

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