Göteborg: Research Scientist, High-Throughput Omics & Safety Innovation

Hitta ansökningsinfo om jobbet Research Scientist, High-Throughput Omics & Safety Innovation i Göteborg. Är det intressant kan du gå vidare och ansöka jobbet. Annars kan du klicka på arbetsgivaren eller yrkesbenämningen för att se alla jobb i Göteborg inom den kategorin.

Publicerad: 2026-01-09 // Varaktighet: Heltid

Make a more meaningful impact to patients' lives around the globe

At AstraZeneca, you'll have the opportunity to make a meaningful difference to patients' lives. With science at its heart, this is the place where breakthroughs born in the lab become transformative medicines - for the world's most complex diseases. Answer unmet medical needs by pioneering the next wave of science, focusing on outcomes and shaping the patient ecosystem.

Join a key international site for AstraZeneca. Discover countless opportunities to grow and develop your personal career, experience and skills.

Always advancing our scientific knowledge and helping to shape the future of healthcare for the greatest and swiftest impact on disease.

We are seeking highly motivated, skilled Scientists with experience in Molecular Biology, Automation and Omics sequencing technologies.

You will perform in vitro omics-enabled safety assessment by generating large-scale, high-throughput transcriptomics to seek a mechanistic understanding of toxicities from projects developing novel medicines.

You will have the opportunity to work closely with a team of Scientists to apply ground-breaking Omics technologies and push the boundaries of predictive safety science with our vision in mind: to deliver innovative safety science to help restore patient's lives.



About the Role

This lab-based, cross-functional role spans the Safety Innovation and NGS/Transcriptomics teams at AstraZeneca R&D in Gothenburg, Sweden. The role is a 12-month temporary assignment, ideally starting in March or April 2026. In this role, you will contribute to our omics-enabled safety assessment efforts by generating large-scale, high-throughput transcriptomics data that supports critical safety decision-making in drug discovery and development. You'll help deliver robust data that underpins projects across therapy areas.

You will work with state-of-the-art automation and sequencing technologies, ensuring that the data underpinning our drug discovery pipeline is of the highest quality.



Your Impact & Responsibilities

*

Execute end-to-end NGS/Transcriptomics workflows, from sample handling to library preparation and sequencing.
*

Gain hands-on experience with automated liquid handling platforms in 384-well plate formats.
*

Perform rigorous quality control (QC) on libraries and sequencing runs to ensure data integrity.
*

Contribute to the development and refinement of evolving sequencing protocols as technology advances.
*

Work closely with scientists from different functions to deliver data-driven insights.



Who You Are

We are looking for a motivated scientist with a "can-do" attitude and a high level of precision. You should be comfortable in a fast-paced lab environment and possess.



Essential Requirements

*

BSc or MSc in Molecular Biology, Biotechnology, Genomics, or a related life science discipline.
*

A lab-based hands-on experience working with NGS assays, especially RNA-Seq.
*

Strong attention to detail, excellent record-keeping skills, and a genuine interest in high-throughput technologies and automation.
*

Applicants must have the eligibility to work in Sweden for 12 months from the start date (estimated March/April 2026).



When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.


So, what's next?

Are you ready to make a meaningful and lasting difference? Apply today and join us in our mission to push the boundaries of science and transform medicine! Please submit your application, preferably both a resume and a cover letter, no later than 25th January 2026.

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Andra jobb i Göteborg som Biolog

Nedan visas andra jobb i Göteborg som Biolog.

Associate Director - Cardiac Safety (In Vitro)

Läs mer Jan 8
At AstraZeneca, we turn bold science into life changing medicines. This is a place where ambitious ideas meet innovative technology, and collaboration makes the impossible possible! Within our Clinical Pharmacology and Safety Sciences (CPSS) function, Safety Innovation designs, selects, and develops safer medicines across the pipeline, from first in class discovery to late-stage development.

We are now seeking an Associate Director, Cardiac Safety (In Vitro), to join our team in Gothenburg, strengthening our Cardiovascular Safety group at the intersection of advanced biology, novel modalities, and translational safety to directly impact patient lives. The position is located at our Gothenburg site, a truly inspiring place to work and home to more than 2,400 colleagues representing over 50 countries. Here, the legacy and the next era of scientific breakthroughs come together. We believe diversity among our people is key to turning discoveries into reality.

About the role

As Associate Director, Cardiac Safety, you will be a scientific leader driving discovery and safety evaluation for novel therapies across AstraZeneca's therapy areas. You will deploy and evolve modern in vitro systems and new approach methodologies (NAMs). You will integrate deep phenotyping, including multiomics, high content imaging, and computational insights. This work aims to solve complex cardiovascular safety questions. This hands-on, high-impact role involves composing strategy and running specific experiments. You will translate mechanisms into decisions to speed innovation safely.

What you will do

Lead custom in vitro safety strategies. Build, perform, and interpret investigational and mechanistic studies to predict, assess, and reduce cardiovascular risks related to targets and chemistry. This enables confident, data-driven progression.

* Drive delivery across multiple projects: Prioritize and balance speed with scientific rigor to meet Cardiac Safety group objectives and portfolio needs.
* Provide expert counsel: Advise project teams and governance on cardiac biology and safety, shaping decisions with high quality data and clear narratives.
* Build next generation models: Characterize and validate advanced in vitro models and NAMs to elevate translational relevance in risk assessment.
* Innovate and influence: Develop and implement novel cardiovascular safety solutions, methods, and proposals that push scientific boundaries while aligning with business and regulatory needs.
* Share and showcase impact: Publish in high quality journals and present at internal and external forums, amplifying AstraZeneca's leadership in cardiovascular safety science.

Essential Requirements

* Degree in Biological Sciences with proven experience, or a PhD with deep understanding of cardiac biology or toxicology; equivalent expertise considered.
* Proven experience in drug discovery and/or toxicology, with a strong record of independent research in industry, biotech, or academia.
* Demonstrated ability to compose, build, and complete in vitro studies evaluating therapeutic effects in complex biological systems.
* Strong background in building, qualifying, and validating complex laboratory-based models with translational endpoints.
* Evidence of leadership through recent publications and experience leading manuscript drafting and peer review.

To succeed in this role, you will bring the following:

* Team oriented, reliable, and results focused; contributes to an open, positive, and inclusive environment.
* Excellent communication and presentation skills, with strong customer and collaborator management; committed to continuous development.
* Ability to challenge conventional thinking and implement creative ideas, balanced with strong understanding of AstraZeneca's regulatory framework.
* Commitment to Good Laboratory Science, Safety, Health and Environment standards, and relevant external regulations.

Why join us?

Step into a role where you will build the future of cardiac safety science with pioneering platforms and data-rich approaches. You will convert complex biology into clear, actionable safety decisions to help bring breakthrough medicines to patients faster. Along the way, you will grow your impact on a global stage, collaborating across a truly international, matrixed organisation where bold ideas travel fast and genuinely matter.

What's next?

If this role sounds interesting to you, please apply with your cover letter and CV by 18 January 2026. We will review applications after the closing date and aim to hold interviews toward the end of January.



Find out more about AstraZeneca Sweden here: https://careers.astrazeneca.com/sweden

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Tjänstebenämning

Läs mer Dec 16
Göteborgs universitet möter samhällets utmaningar med mångsidig kunskap. 58 000 studenter och 6800 medarbetare gör universitetet till en stor och inspirerande arbetsplats. Stark forskning och attraktiva utbildningar lockar forskare och studenter från hela världen. Med ny kunskap och nya perspektiv bidrar Göteborgs universitet till en bättre framtid.

Information om anställningen hittar du på Göteborgs universitets websida: https://web103.reachmee.com/ext/I005/1035/job?site=6&lang=SE&validator=3038fcf1516ea1184a6da70a891f87da&job_id=39140




Universitetet tillämpar lokalt avtal om lönesättning av doktorander.


 

Du ansöker via https://www.gu.se/om-universitetet/jobba-hos-oss/lediga-anstallningar

.


Universitetet arbetar aktivt för en arbetsmiljö med jämställda förhållanden och sätter värde på de kvalitéer mångfald tillför verksamheten. Universitetet tillämpar individuell lönesättning.

 

 

Lägg till att man ansöker via https://www.gu.se/om-universitetet/jobba-hos-oss/lediga-anstallningar

.

Universitetet arbetar aktivt för en arbetsmiljö med jämställda förhållanden och sätter värde på de kvalitéer mångfald tillför verksamheten.

Universitetet tillämpar individuell lönesättning.

Enligt Riksarkivets föreskrifter är universitetet skyldigt att förvara ansökningshandlingar i två år efter tillsättningsbeslutet. Om du som sökande till en anställning särskilt begär tillbaka dina handlingar återsänds de när de två åren har förflutit, i annat fall kommer de att gallras ut.

Till bemannings- och rekryteringsföretag och till dig som är försäljare: Göteborgs universitet anlitar upphandlad annonsbyrå i samband med rekrytering av personal. Vi undanber oss vänligen men bestämt direktkontakt med bemannings- och rekryteringsföretag samt försäljare av jobbannonser.

Ansök nu

Erfaren forskare inom Hållbart Jordbruk

Läs mer Dec 8
Brinner du för att utveckla ett mer hållbart jordbruks- och livsmedelssystem och vill göra det tillsammans med forskare, företag, myndigheter och andra samhällsaktörer? Då kan du vara rätt person hos oss!
Enheten Hållbara Matsystem samlar omkring 20 forskare och specialister som arbetar för en hållbar omställning av matsystemet genom tillämpad och lösningsorienterad forskning. Genom systemanalytiskt och tvärvetenskapligt arbete och i nära samverkan med näringsliv, offentlig sektor och akademi utvecklar vi kunskap, data och metoder som möjliggör hållbara beslut i hela livsmedelskedjan – från hav och jord till bord.
Om rollen Vi söker nu en erfaren forskare som vill bidra till och vidareutveckla vår forskning och våra uppdrag inom området hållbart jordbruk. I dag arbetar 7–8 personer i gruppen med frågor inom exempelvis växtproduktion, djurens roll i hållbara livsmedelssystem, biologisk mångfald, miljöindikatorer, klimatberäkningar, jordhälsa och metodutveckling inom LCA. Vi samverkar också brett inom RISE med kompletterande kompetenser.
Vårt arbete omfattar alltifrån fleråriga nationella och internationella forskningsprojekt till kortare uppdrag för företag, myndigheter och miljöorganisationer. Vi tar ett gemensamt ansvar för att utveckla området och ser till helheten snarare än individuella projekt.
Som forskare inom hållbart jordbruk hos oss kommer du att:
Vara drivande i utvecklingen av forskningsområdet hållbart jordbruk
Leda egna forskningsprojekt och bidra i andras
Initiera och driva ansökningar, både självständigt och i samverkan med kollegor och externa parter
Arbeta strategiskt med att utveckla området på både kort och lång sikt
Genomföra kortare kunduppdrag inom din och gruppens expertis
Representera RISE i relevanta forum internt och externt

Tjänsten är placerad på enheten Hållbara Matsystem inom RISE Livsmedelsavdelning, med placering i Göteborg, Lund eller Uppsala. Observera att denna tjänst kan innebära att en säkerhetsprövning krävs, antingen senare i denna process eller i framtiden.
Vem är du? Vi söker dig som:
är disputerad agronom, biolog, ekolog, miljövetare eller liknande, med minst tre års arbetslivserfarenhet efter disputation
har dokumenterad erfarenhet av att driva egna projekt och forskningsansökningar
har god kunskap om det svenska jordbrukssystemet och dess miljöpåverkan
är van vid projektledning och projektskapande
uttrycker dig väl i tal och skrift på svenska
behärskar engelska obehindrat

Det är också meriterande om du har:
erfarenhet av LCA och/eller andra systemvetenskapliga metoder för miljövärdering av jordbruk och primärproduktion
erfarenhet av att utveckla metoder och/eller modeller för olika typer av hållbarhetsbedömningar
erfarenhet av tillämpade projekt så att du kan agera brygga mellan forskningen och näringen
ett etablerat nätverk inom forskningsområdet, nationellt och gärna internationellt

Som person är du prestigelös, social och trivs i ett team där vi löser komplexa utmaningar tillsammans. Du tar initiativ, bidrar med energi och inspireras av samarbete i tvärvetenskapliga miljöer. Vidare är du analytisk, noggrann och levererar med hög kvalitet. Då många av våra partners är internationella behöver du även behärska engelska obehindrat.
Är vi rätt för varandra? På RISE värdesätter vi olikheter, och vi är övertygade om att mångfald skapar en innovativ miljö där vi tillsammans utvecklar ny kunskap och bidrar till en mer hållbar framtid. Hos oss samlas engagerade problemlösare som arbetar med några av vår tids största samhällsutmaningar. Här får du goda möjligheter att utvecklas både professionellt och personligt.
Välkommen med din ansökan! Om du har frågor är du välkommen att kontakta Maria Hellström, enhetschef, +46 10 516 66 30 eller Ulf Sonesson, forskare, +46 10 516 66 17. Sista ansökningsdag är 9 jan 2026 men vänta inte med din ansökan då urval och intervjuer kan komma att ske löpande under ansökningsperioden.
Våra fackliga representanter är Ingemar Petermann, SACO +46 10 228 41 22 och Linda Ikatti, Unionen, +46 10 516 51 61.
Forskning, RISE, jordbruk, hållbarhet, LCA, miljö, klimat, biologisk mångfald, agronom, markanvändning, ekolog, biolog, jordhälsa, livsmedel, Uppsala, Göteborg, Lund

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Associate Director - Cardiac Safety (In Vitro)

Läs mer Dec 8
At AstraZeneca, we turn bold science into life changing medicines. This is a place where ambitious ideas meet innovative technology, and collaboration makes the impossible possible! Within our Clinical Pharmacology and Safety Sciences (CPSS) function, Safety Innovation designs, selects, and develops safer medicines across the pipeline, from first in class discovery to late-stage development.



We are now seeking an Associate Director, Cardiac Safety (In Vitro), to join our team in Gothenburg, strengthening our Cardiovascular Safety group at the intersection of advanced biology, novel modalities, and translational safety to directly impact patient lives. The position is located at our Gothenburg site, a truly inspiring place to work and home to more than 2,400 colleagues representing over 50 countries. Here, the legacy and the next era of scientific breakthroughs come together. We believe diversity among our people is key to turning discoveries into reality.



About the role

As Associate Director, Cardiac Safety, you will be a scientific leader driving discovery and safety evaluation for novel therapies across AstraZeneca's therapy areas. You will deploy and evolve modern in vitro systems and new approach methodologies (NAMs). You will integrate deep phenotyping, including multiomics, high content imaging, and computational insights. This work aims to solve complex cardiovascular safety questions. This hands-on, high-impact role involves composing strategy and running specific experiments. You will translate mechanisms into decisions to speed innovation safely.



What you will do

Lead custom in vitro safety strategies. Build, perform, and interpret investigational and mechanistic studies to predict, assess, and reduce cardiovascular risks related to targets and chemistry. This enables confident, data-driven progression.

* Drive delivery across multiple projects: Prioritize and balance speed with scientific rigor to meet Cardiac Safety group objectives and portfolio needs.
* Provide expert counsel: Advise project teams and governance on cardiac biology and safety, shaping decisions with high quality data and clear narratives.
* Build next generation models: Characterize and validate advanced in vitro models and NAMs to elevate translational relevance in risk assessment.
* Innovate and influence: Develop and implement novel cardiovascular safety solutions, methods, and proposals that push scientific boundaries while aligning with business and regulatory needs.
* Share and showcase impact: Publish in high quality journals and present at internal and external forums, amplifying AstraZeneca's leadership in cardiovascular safety science.



Essential Requirements

* Degree in Biological Sciences with proven experience, or a PhD with deep understanding of cardiac biology or toxicology; equivalent expertise considered.
* Proven experience in drug discovery and/or toxicology, with a strong record of independent research in industry, biotech, or academia.
* Demonstrated ability to compose, build, and complete in vitro studies evaluating therapeutic effects in complex biological systems.
* Strong background in building, qualifying, and validating complex laboratory-based models with translational endpoints.
* Evidence of leadership through recent publications and experience leading manuscript drafting and peer review.



To succeed in this role, you will bring the following:

* Team oriented, reliable, and results focused; contributes to an open, positive, and inclusive environment.
* Excellent communication and presentation skills, with strong customer and collaborator management; committed to continuous development.
* Ability to challenge conventional thinking and implement creative ideas, balanced with strong understanding of AstraZeneca's regulatory framework.
* Commitment to Good Laboratory Science, Safety, Health and Environment standards, and relevant external regulations.



Why join us?

Step into a role where you will build the future of cardiac safety science with pioneering platforms and data-rich approaches. You will convert complex biology into clear, actionable safety decisions to help bring breakthrough medicines to patients faster. Along the way, you will grow your impact on a global stage, collaborating across a truly international, matrixed organisation where bold ideas travel fast and genuinely matter.



What's next?

If this role sounds interesting to you, please apply with your cover letter and CV by 7 January 2026. We will review applications after the closing date and aim to hold interviews toward the end of January.



Find out more about AstraZeneca Sweden here: https://careers.astrazeneca.com/sweden

Ansök nu

Andra jobb i Göteborg från Astrazeneca AB

Nedan visas andra jobb i Göteborg från Astrazeneca AB .

Principal Research AI Engineer - Center for AI

Civilingenjör, systemutveckling
Läs mer Jan 15
Nytt
Lead the next wave of AI Innovation
Join AstraZeneca's Center for AI and push the boundaries of what's possible. We combine cutting-edge science with advanced AI to accelerate discoveries and deliver life-changing medicines. Here, you'll work with visionary minds, explore bold ideas, and shape the future of healthcare through technology. Innovation starts with you.


The role is to bridge cutting-edge AI research and production engineering, enabling scientific breakthroughs through robust, scalable, and sustainable research infrastructure. This position provides strategic technical leadership in building the platforms, tools, and practices that accelerate AI-driven scientific discovery while championing sustainability and engineering excellence across AstraZeneca's R&D and Science functions.


Key Accountabilities

Research Engineering Leadership

* Provide technical vision and leadership for research engineering initiatives that enable scientists and researchers to rapidly experiment, iterate, and scale AI solutions from concept to production

* Design and implement research infrastructure, frameworks, and tooling that bridge the gap between exploratory research and enterprise deployment, ensuring reproducibility, scalability, and compliance

* Mentor research engineers and collaborate closely with research scientists to establish best practices that maintain scientific rigor while accelerating the path from research to impact


Sustainable AI Research Infrastructure

* Lead the definition and implementation of sustainability strategies for AI research workloads, establishing metrics, monitoring frameworks, and optimization practices to minimize environmental impact without compromising scientific quality

* Architect efficient distributed computing solutions for large-scale model training and experimentation across cloud and on-premises infrastructure, optimizing for both performance and energy efficiency

* Drive innovation in resource utilization, experiment tracking, and computational efficiency to reduce costs and carbon footprint of research activities


Research-to-Production Excellence

* Own the research engineering standards and practices within AI for Science, developing comprehensive documentation, reusable components, and automation that enable seamless transition from research prototypes to production systems

* Partner with research teams, infrastructure groups, MLOps teams, and external collaborators to create robust pipelines that support the full research lifecycle from hypothesis to validated, deployable solutions

* Accelerate scientific discovery by implementing DevOps, GitOps, and MLOps automation tailored to research workflows, reducing friction and manual intervention while maintaining experimental flexibility

Innovation and Scientific Enablement

* Identify and evaluate emerging research engineering methodologies, tools, and technologies that enhance both scientific capability and operational sustainability

* Lead initiatives to improve reproducibility, experiment management, and collaboration across distributed research teams

* Foster a culture of innovation that balances scientific exploration with engineering discipline, enabling researchers to focus on discovery while maintaining production-quality standards


Essential Skills and Experience

* PhD in Computer Science, Engineering, or a relevant scientific field, or Master's degree with significant experience in research engineering or applied research roles

* Demonstrated track record of building research infrastructure and tooling that has enabled scientific teams to achieve measurable impact

* Extensive experience establishing research engineering best practices, including experiment tracking, reproducibility frameworks, and research-to-production workflows

* Expertise in automating research workflows and the machine learning lifecycle, with focus on enabling rapid experimentation and iteration

* Advanced proficiency in Python and the scientific computing ecosystem (NumPy, Pandas, SciPy, etc.), with understanding of how researchers use these tools

* Expert-level experience with PyTorch or similar frameworks, including implementing custom architectures and optimizing training workflows

* Demonstrable Experience with DDP, FSDP and multi-node training.

* Strong background with modern DevOps practices including GitHub/GitLab, CI/CD pipelines, and infrastructure-as-code applied to research environments

* Experience with running workloads as containers, container orchestration, cloud and on-prem workloads.

* Demonstrated ability to collaborate effectively with research scientists, translating research needs into robust engineering solutions

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Associate Director, Clinical Regulatory Writing

Bioinformatiker
Läs mer Jan 14
Are you passionate about transforming science into clear and compelling regulatory documents that drive successful drug development? We are seeking a talented and experienced Associate Director, Clinical Regulatory Writing to join our CVRM (Cardiovascular, Renal and Metabolism) Clinical Regulatory Writing team in Gothenburg, Sweden. With more than 2,400 employees from over 50 countries, our vibrant Gothenburg site is a truly inspiring place to work - where the history and future of scientific breakthroughs come together. We believe that the diversity of our people is crucial to bringing new discoveries to life.



Accountabilities:

The CVRM Clinical Regulatory Writing group provides expert strategic leadership and communications expertise to clinical drug programs, ensuring delivery of high-quality, label-focused documents aligned with project strategy, regulatory requirements, and communications best practices. Role holders not only author critical clinical-regulatory documents but also act as critical reviewers to achieve the highest quality standards. Team members also represent the Clinical Regulatory Writing skill set on both drug and non-drug projects, advocating for best practices and continuous improvement.



Key Responsibilities

As an Associate Director, Clinical Regulatory Writing, you will:

*

Provide strategic leadership and communication expertise to clinical drug programs across the CVRM portfolio.
*

Author and critically review clinical-regulatory documents, ensuring the highest regulatory, technical, and quality standards.
*

Represent Clinical Regulatory Writing on project teams, advocating for communication best practices.
*

Provide strategic communications leadership within clinical delivery or submission teams, establishing standards and promoting quality and efficiency.
*

Act as NDA/MAA submission lead, driving the development of the clinical Submission Communication Strategy (cSCS) and successful submission delivery.
*

Lead both internal and external authoring teams and cultivate strong partnerships with vendor medical writers to ensure timely, high-quality document delivery.
*

Translate complex clinical data into clear, concise, and accurate messages tailored to specific audiences.
*

Support the development and upskilling of colleagues within the Clinical Regulatory Writing function.
*

Champion continuous improvement and operational excellence in communications.



Essential Skills/Experience:

*

Bachelor's degree in Life Sciences or a related discipline.
*

Significant medical writing experience within the pharmaceutical industry or a Contract Research Organization (CRO).
*

Proven ability to advise and lead communications projects and teams.
*

Strong understanding of drug development and the communications process from early development through to launch and lifecycle management.
*

In-depth knowledge of technical and regulatory requirements relevant to clinical regulatory writing.



Desirable Skills/Experience:

*

Advanced degree in scientific discipline (e.g., Ph.D.).



If you are driven to deliver impactful regulatory communications, excel in multidisciplinary teams, and want to shape the future of clinical development, we encourage you to apply.

Apply with your CV and cover letter by 31 January!

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Senior Scientist Integrated Bioanalysis, Immunoassay Specialist

Molekylärbiolog
Läs mer Jan 14
About Discovery Bioanalysis

Discovery Bioanalysis (DxBA) is a global department within Integrated Bioanalysis, Clinical Pharmacology & Safety Sciences, supporting AstraZeneca's portfolio from early discovery through clinical development. The team applies advanced analytical technologies, including immunoassay, quantitative LC-MS, flow cytometry, multi-omics, and spatial biology to generate high-confidence datasets for decision-making at key project milestones.

Discovery Bioanalysis is responsible for developing and implementing bioanalytical strategies, ensuring robust and reliable data to guide candidate selection and program progression. Working closely with cross-functional project-teams, the group provides comprehensive support across discovery, preclinical, and clinical phases, contributing to the advancement of therapies for complex diseases.



About the role

This is an opportunity for a motivated immunoassay expert to join our Integrated Bioanalysis (IBA) team in Gothenburg (Sweden) as a Senior Scientist.

As part of the Discovery Bioanalysis Team, you will develop and validate bespoke immunoassays to assess pharmacokinetics and target engagement biomarkers across diverse therapeutic modalities. The role involves designing, executing, and transferring complex assays using advanced instrumentation to support discovery, preclinical and clinical studies. You will ensure assays are fit for purpose to meet their intended context of use & will collaborate with internal and external partners, reviewing and analyzing data; and troubleshooting assay performance. As a Subject Matter Expert, you will be responsible for enhancing the IBA reputation for scientific excellence by presenting at internal and external meetings, and publishing manuscripts.

Alongside the core laboratory role you will have the opportunity as a Discovery Bioanalytical lead to work within a dynamic cross-functional team in a matrixed environment, defining and executing on tailored & focused project-specific bioanalytical strategies supporting decision-making and advancing the pipeline. You will work in close partnership with key stakeholders across the business, input to project strategy and delivery, managing expectations whilst interfacing with experienced and highly skilled bioanalytical scientist colleagues or our partnered labs. You will have the opportunity to influence decisions from early discovery through late-stage development and have an immediate and lasting impact to our diverse pipeline.



Essential requirements:

*

PhD or MSc (1-3 years' experience), or BSc (3+ years' experience) in immunology, molecular biology, or related field with significant relevant experience.
*

Proven expertise as a subject matter expert in ligand-binding immunoassay techniques (expert level for MSD plus one of: Gyrolab, Simoa, SMC-Pro, NULISA, Ella).
*

Demonstrated experience in leading bioanalytical project strategy.
*

Experience developing robust, state-of-the-art assays for bioanalytical characterization of pharmacokinetics in preclinical and clinical studies, including complex large molecule bioanalysis (e.g., multi-specific antibodies, T cell engagers).
*

Expertise in target engagement and occupancy biomarker assay development, including fit-for-purpose approaches.
*

Demonstrated experience with total and free assay development to support dose modelling.
*

Bioanalytical support for non-GLP IND-enabling studies, including assay qualification and tech transfer for GxP-like and GxP studies.
*

Ability to independently design, execute, and troubleshoot assays.
*

Proficient in data analysis using Softmax Pro and MSD Workbench.
*

Maintain high-quality documentation in electronic lab notebooks and prepare technical reports for regulatory submissions.
*

Interpret complex datasets for key project decisions as part of cross-functional, multi-platform teams.
*

Effective collaboration in a matrix environment and presentation of findings to scientific and management audiences.
*

Agile and adaptable, able to manage multiple projects in a fast-paced setting.
*

Strong publication record, communication, and organizational skills; proven accountability and teamwork.



Desirable for the role:

*

Experience implementing AI and automation in laboratory and data workflows.
*

Experience with ultrasensitive immunoassay platforms (e.g., Simoa, SMC-Pro, NULISA).
*

Experience across additional analytical platforms (e.g., spatial, circulatory, molecular technologies such as imaging, cytometry, PCR).
*

Background in developing and executing multiplexed immunoassays on Luminex.
*

Previous involvement in pharmaceutical research with comprehensive understanding of drug discovery phases and related bioanalytical requirements.
*

Basic coding skills for laboratory and data automation.



When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of four days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.



Ready to make an impact?

Are you ready to make a meaningful and lasting difference? Apply today and join us in our mission to push the boundaries of science and transform medicine. Please submit your application; CV and cover letter, between 15 January 2026 and 28 February 2026.

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Clinical Pharmacology Scientist, CVRM

Forskare, farmakologi
Läs mer Jan 13
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.



What you will do

This is an opportunity for an engaged individual to join our Clinical Pharmacology and Quantitative Pharmacology (CPQP) team at AstraZeneca in Gothenburg (Sweden) and contribute as an Associate Director Clinical Pharmacology Scientist, supporting large and small molecule projects across all phases of clinical development within the therapy area of Cardiovascular Renal and Metabolism.

You will work closely with clinical pharmacometricians, physicians and other scientists, and apply your expertise and leadership skills to contribute to the strategy of the clinical program and the design and interpretation of clinical studies. You will influence key decisions in early and late phases of clinical development. Accountable for expert data integration, analysis, interpretation, and reporting of clinical pharmacology results at the study level in compliance with Good Clinical Practice (GCP) regulations. Jointly accountable with the clinical pharmacometrician for providing a scientific justification for the dose selection, for representing Clinical Pharmacology and Quantitative Pharmacology in cross-functional project teams, and for developing the clinical pharmacology strategy. Participation in and accountability for peer review of ongoing activities, reports and presentations. Contribute to regulatory documents and interactions (written and oral), present Clinical Pharmacology results within and outside of AstraZeneca and publish in peer reviewed journals. You will also contribute to internal initiatives to develop the clinical pharmacology field including its processes.



Essential requirements for this role

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PhD degree in clinical pharmacology, pharmacometrics or other relevant area
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Strategic knowledge and experience applying clinical pharmacology in clinical drug development
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Knowledge of pharmacokinetics, drug metabolism, and their clinical application
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Knowledge in pharmacology and drug targets
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At least 3 years industry experience in pharmacokinetics and clinical pharmacology aspects of drug development
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Good oral and written communication skills



Desirable requirements

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Biological understanding of disease and drug action in the therapy area of Cardiovascular Renal and Metabolism
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Early and late phase clinical development experience
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Track record in creating and delivering on clinical pharmacology strategies of both small and large molecules
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Recognized clinical pharmacology expert as demonstrated by scientific publishing in the field of clinical pharmacology
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Skills and experience in the use of PK and PKPD modeling tools such as Phoenix Winnonlin, NONMEM, R applied to life sciences



When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.


So, what's next?

If you're ready to make a meaningful, lasting impact, apply today and help us push the boundaries of science to transform medicine.

Please submit your application, ideally including both a resume and a cover letter, by 31January, 2026. We review applications on a rolling basis, so we encourage you to apply as soon as possible.

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Modelling and Simulation PK/PD Expert

Bioinformatiker
Läs mer Jan 9
Are you a passionate individual with expertise in mathematical modelling and pharmacokinetics-pharmacodynamics (PK/PD)? Do you want to contribute to the development of future treatments for cardiovascular, renal, and metabolic diseases? If so, we invite you to join our Modelling & Simulation team within the Early Cardiovascular, Renal and Metabolism (CVRM) therapeutic area at AstraZeneca. This position is based at our dynamic R&D site in Gothenburg, Sweden.



Accountabilities:

As a Modelling and Simulation PK/PD expert, you will play a key role in shaping project strategies and driving critical decisions across our drug discovery portfolio. You will actively influence drug project teams, guiding the selection of targets, molecules, optimal dosing strategies, patient populations, and overall development pathways.

You will have the opportunity to design and oversee the execution of complex studies in preclinical disease models, applying advanced mathematical modelling approaches to deliver impactful PK/PD and translational insights. Your expertise will enable you to synthesize data from multiple sources, predict human pharmacokinetics and pharmacodynamics, and influence the definition of efficacious exposure and dosing regimens.

In this role, you will present and defend your quantitative assessments and recommendations to internal governance and senior stakeholders, shaping critical decisions at the highest levels. You will also provide scientific leadership by initiating and leading strategic DMPK and PK/PD innovation projects, fostering collaboration across disciplines, and representing AstraZeneca's modelling expertise both internally and within the broader scientific community.



Essential Skills/Experience:

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PhD in pharmacokinetics, pharmacology, mathematics, or related field, with a focus on model-based PK/PD approaches, preferably in a preclinical/translational setting

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Industry or academic experience in exposure-response modelling (PK/PD, NLME, PBPK and/or QSP) including hands-on experience with scriptable modelling softwares (e.g., Phoenix, R, Matlab, Python, Monolix, NONMEM)

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Demonstrated scientific leadership through a publication track record in relevant area

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Excellent interpersonal skills and the ability to work in cross-functional teams

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Excellent communication skills in English, both verbal and written



Desirable Skills/Experience:

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Experience in pharmaceutical research and development

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Experience in defining quantitative modelling strategies across various therapeutic modalities (e.g., small molecules, oligonucleotides, peptides, proteins, antibodies or cell/gene therapy)
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Experience applying AI/machine learning to research workflows, including data curation, PK/PD or translational modeling
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Experience in PBPK modelling (e.g. Simcyp or PK-Sim)



At AstraZeneca, we are driven by results and use our unique blend of science and commercial knowledge to spot opportunities and drive outcomes. We are part of an expansive healthcare ecosystem that connects key players across the entire patient journey. Our patient-first approach informs every decision we make. We are committed to your development and believe that your best is better here. Join us and be part of a global team filled with the smartest minds.



Ready to make your mark? Apply now and be a part of our journey to redefine the future of healthcare! Welcome with your application no later than January 25th, 2026.

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