Recruitment assignments
See additional recruitment projects in Swedish on our Swedish website.
Choose category
Do you want to work at a leading clinical-stage biotech company contributing to the advancement of modern innovative medicines based on our highly innovative Affibody® protein therapeutics technology?
We are looking for you who wants to be part of the development of new biopharmaceuticals and who wants to help drive science and product development at a successful and expanding biotech company. You will focus on forecast, plan and overseeing the supply of Investigational and Non-Investigational Drugs and auxiliary materials. it is a broad position with broad responsibility having impact on large areas of development.
Do you want to devote yourself taking part in the work developing new drugs for patients with severe kidney disease with no cure today? You will work with development of a treatment for a disease that particularly strike children.
Do you want to devote yourself taking part in the work developing new drugs for patients with severe kidney disease with no cure today? You will work with development of a treatment for a disease that particularly strike children.
Do you want to devote yourself taking part in the work developing new drugs for patients with severe kidney disease with no cure today? You will work with development of a treatment for a disease that particularly strike children.
Your work is to manage a team with a broad scope including Sourcing and supply, Management of GMP processes, QC analyses, CMC Regulatory and Budget and resources.
Do you want to contribute to the development of bioanalytical immunology work at Sobi as a Senior Scientist?
Sobi is currently looking for a Senior Scientist Bioanalytical Immunology to join Sobi Bioanalysis section within R&D. The section is responsible for bioanalysis throughout all stages of preclinical and clinical development. The work is focused on biotechnology products and performed in cross-functional teams in a highly collaborative, experienced and engaged environment.
The Associate Director/Director Preclinical Development will manage preclinical project activities to successful and timely delivery from internal process- and assay development, via outsourcing to contract manufacturing organizations and contract research organizations for IND enabling studies up to the regulatory documentation needed for the clinical translation of Affibody projects.
The Research Engineer Protein Purification will focus on purification of Affibody® molecules, in Affibody’s research pipeline, as well as in downstream process development after CD selection. He or she will plan and execute experiments, perform in-process analyses, analyze data, and report results to meet specified timelines and objectives.
The Research Engineer Protein Expression will focus on expression of Affibody® molecules, in Affibody’s research pipeline, as well as in upstream process development after CD selection. He or she will plan and execute experiments, perform in-process analyses, analyze data, and report results to meet specified timelines and objectives.
Do you want to support clinical studies and projects with Clinical Data Management skills and Project Management all the way to submission?
Do you want to be part of the development of new protein therapeutics at an innovative, exciting and expanding biotech company and help drive science to patients?
Do you want to be part of the development of new protein therapeutics at an innovative, exciting and expanding biotech company and help drive science to patients?
Do you have experience from work in the pharmaceutical industry with protein drug development and analytical chemistry?
Do you want to be part of the development of new protein therapeutics at an innovative, exciting and expanding biotech company and help drive science to patients?
We are looking for you who wants to be part of the development of new pharmaceuticals and who wants help drive science at a successful and expanding pharmaceutical company. You will focus on immunogenicity assessments, method development and bioanalysis of protein therapeutics, including out-sourcing of methods to support regulatory preclinical and clinical studies and out-sourced GMP production.
Do you want to take part in bringing pharmaceutical projects from ideas to approved drugs? Look further into this and contact us if you are a talented cancer biologist wanting to support this exciting effort by working on this permanent position in Medivir.
This an exciting opportunity for you who wants to be part in bringing pharmaceutical products to the market place bringing cure to important medical needs. We are searching for a person who can take responsibility for Drug Process Support and Manufacturing.
This is an opportunity for you who have experience from process development and manufacturing within the biotech industry.
This an exciting opportunity for you who wants to be part in bringing pharmaceutical products to the market place bringing cure to important medical needs. We are searching for a person who can take responsibility for Drug Product Support and Analytics.
This is an opportunity for you who have experience from formulation development work as well as competence within analytical method development and validation.
Aktivia Science Work is seeking a Protein Crystallization Scientist working with the generation of single crystals of proteins and protein-ligand complexes for X-ray structure determination for Medivir projects.
Do you want to be responsible for overall coordination and management of clinical trials from startup to closeout according to the protocol and study plan at an exciting vaccines company?
The Scientist Lead Generation Protein Drugs will focus on lead generation of Affibody molecules in Affibody’s research pipeline and characterization of binding interactions.
Medivir is seeking a Protein NMR Specialist to join the Computational Chemistry and Structural Biology department
We are searching for a person to be part of Eurocine Vaccines R&D team being responsible of all CMC aspects in company R&D projects contributing to develop the company technical platform as well as the vaccine project.
Do you want to be part in a growing and evolving company developing next generation biopharmaceuticals?
We are now searching for an experienced Senior Clinical Project Manager for recruitment to Medivir in Huddinge, just south of Stockholm. You will be part of Clinical Operations and will have responsibility for program lead and clinical project management for all operation activities within a program or project/projects. You will ensure a well-functioning study team and will be a contributor to strategic planning as well as to licensing and similar Business Development activities.
We are now searching for an experienced Senior Clinical Trial Associate (CTA) for recruitment to Medivir in Huddinge, just south of Stockholm. You will have responsibility to manage all kind of administrative and logistic support to Clinical Operations and the different clinical studies that are conducted by the company.
Our client company needs a CMC Project Leader with experience from small molecule work due to more and more project activities and increasing need of manufacturing of both Drug Substances and Drug Products
Do you want to be part of a growing and developing business expanding with new products, new customers and presence at a growing international market?
Medivir is seeking an experienced Senior Research Scientist to join the Chemistry Department which provides design and synthesis of new compounds to Medivir discovery projects and the R&D organisation. You will be located at Medivir R&D site in Huddinge (just outside of Stockholm) and report to the Associate Director Chemistry.
The Program Director will focus on coordinating and guiding Affibody’s biopharmaceutical programs. This includes hands-on work with preclinical and clinical development program/project planning, operative project activities (clinical trial design) and follow-up to deliver successful and timely milestones/development stages.
The scope includes supporting the management team with coordination and reporting of timelines from CMC/Tox through clinical trials up to outlicensing to partners or commercialization.
Medivir is seeking an experienced Analytical Chemist to support international projects with compound characterization analyses.
The Head of Market Access and External Affairs Sweden shall develop and defend Company image, reputation and interest amongst key external stakeholders and ensure that reimbursement/price submissions to authorities are of high quality and submitted within given timelines.
Sobi are now looking for a Senior Scientist experienced in pharmacokinetics. You will provide pharmacokinetics expertise to support development of new recombinant protein drugs for rare specialist indications to add value for the patient.
We are looking for a Global Regulatory Affairs Director, who will be overall responsible for the regulatory work to obtain and maintain marketing authorizations through submissions and communication to/with regulatory authorities, for both Sobi products and Partner Products. The work requires extensive internal as well as external communication and co-ordination.
Medivir is seeking an experienced Senior Computational Chemist to join the Department of Computational Chemistry and Structural Biology which provides computational chemistry, modeling, chemoinformatic and X-ray crystallography support to the R&D organisation. You will be located at our R&D site in Huddinge (just outside of Stockholm) and report to the Director of Computational Chemistry and Structural Biology.
Albireo is recruiting a CMC Director. In this role you will be is responsible for that adequate drug formulations are available to start of all clinical studies within Albireo and secure that Albireo have satisfactory CMC data set for application of clinical studies and get an approval by authority.
The Medical Writer will work on preparing and completing clinical and regulatory documentation in assigned Study Teams, according to company policies, SOP’s and regulatory requirements.
Your focus will be clinical pharmacology from early-development (pre-IND) through late-stage development (worldwide filings and life cycle management) within the Clinical Pharmacology and DMPK section. The section is responsible for clinical pharmacology as well as DMPK and bioanalysis throughout all stages of preclinical and clinical development.
The Medical Writer is part of the Medical Affairs Department within Project Delivery and will work on preparing and completing clinical and regulatory documentation in assigned Study Teams, according to company policies, SOP’s and regulatory requirements.
We are looking for you who are a computational chemist, preferably at PhD-level. You will analyse the relationship between the variation in chemical structures and biological activities of test substances in Discovery projects. The position involves the use of molecular mechanical and quantum mechanical calculations, pharmacophore modelling, experimental design, QSAR and methods for structure-based drug design. The person we are seeking is creative, takes initiatives and has good team and communication skills.
You will provide in vivo pharmacology expertise to support development of new recombinant protein drugs for rare specialist indications to add value for the patient.
As the Safety Physician you will work in the department responsible for all aspects of patient safety and pharmacovigilance activities for all products and products in development.
You will work in the Drug Design & Development department of Sobi. You will work throughout all stages of preclinical and clinical development as well as clinical pharmacology. The work is focused on biotechnology products and performed in cross-functional teams in a highly collaborative, experienced and engaged environment.
Your main objective will be to take the medical strategic leadership for all medical activities, both science , regulatory and marketing, and be the medical expert and contact person for internal and external stakeholders.
The Senior Health Economist/Market Access Manager provides Sanofi Business Leaders with insight and analyses regarding pricing and health economics for Sanofi products and therapies in Sweden. He or she will also have external contacts with different decision makers in authorities and different Swedish health care organizations.
As part of an expanding business our customer will strengthen the marketing department with a Clinical Product Manager. This will be a key role with focus to introduce new products within the growing business areas companion diagnostics and personalized medicine.
Become part of an internationally expanding speciality laboratory for autoimmune diseases as the new Senior Key Account Manager, an independent role with large degree of influence on how to develop sales and the Sales function.
Medivir is seeking an experienced toxicologist/safety pharmacologist to join the Department of Preclinical Development which plays an important role in the R&D organization at Medivir.
Medivir is seeking an experienced Senior Research Scientist Computational Chemistry to join the Department of Computational Chemistry and Structural Biology which provides computational chemistry, modeling, chemoinformatic and X-ray crystallography support to the R&D organisation. You will be located at Medivir R&D site in Huddinge (just outside of Stockholm) and report to the Director of Computational Chemistry and Structural Biology.
Medivir is seeking an experienced Senior Research Scientist to join the Department of Computational Chemistry and Structural Biology which provides computational chemistry, modeling, chemoinformatic and X-ray crystallography support to the R&D organisation. You will be located at Medivir R&D site in Huddinge (just outside of Stockholm) and report to the Director of Computational Chemistry and Structural Biology.
The CRA Group Head Sweden and Norway shall provide leadership and line management to CRAs in Sweden and Norway.
We are now looking for a Senior Toxicologist with long experience from non-clinical safety in pharmaceutical industry. You will provide non-clinical safety and toxicology expertise to support existing products and development of new recombinant protein drugs for rare specialist indications to add value for the patient.
We are now looking for a Clinical Program Leader (CPL) who has extensive experience in managing global studies in early as well as late phases of clinical development, Life Cycle Management and product support.
The External Affairs Manager secures the development of the Oncology business throughout the Swedish healthcare regions/county councils and identifies relevant stakeholders at the regional and county council level to ensure Oncology drugs are included in the regions.
This is an opportunity to work both on the Scandinavian level as well as on the local Swedish market as Medical lead.
The Franchise Head is responsible for the development, adaption and implementation of global marketing and portfolio strategy for the franchise, key disease areas and/or a range of products and indications.
We are now looking for a Clinical Program Leader (CPL) who has extensive experience in managing global studies in later phases of clinical development including pre-marketing studies.You will manage planning, execution and delivery of late phase clinical studies in the field of hemophilia.
Do you want to be part of the team that put Novartis forward on the Swedish market for novel and innovative pharmaceutical products?
As External Affairs Manager Sweden you establish relationships with regional decision-makers to improve the overall business environment by eliminate regional market hurdles and developing business in the region.
As Commercial Excellence Coordinator you are responsible for providing support to commercial teams in Novartis Oncology Nordic cluster by implementing and coordinating tools and projects. You contribute towards building the best-in-class commercial organization by external and internal benchmarks.
Do you want to be part of the team that put Novartis forward on the Scandinavian market for novel and innovative pharmaceutical products?
As Medical Director Scandinavia you present a strong leadership for the Medical Department in Novartis Country Pharma Organisation (CPO) Scandinavia.
Do you want to be part of the team that put Novartis forward on the Swedish market for novel and innovative pharmaceutical products?
As External Affairs Manager Sweden you establish relationships with regional decision-makers to improve the overall business environment by eliminate regional market hurdles and developing business in the region.
Would you like to take on the challenge to bring Genovis forward by strategic market development combined with real hands-on sales work? Do you have experience of complex sales work within life science and a technical/scientific background in biologics? Then you most certainly are the person we are looking for!
You will be responsible for taking Genovis to the next market level and will be part of Genovis Management Team.
As Head Health Economics Sweden you lead the health economics work and are responsible for adaption of global models and various health economic studies and activities.
As Head of Medical Oncology Sweden you provide leadership to Medical Advisors within all three oncologu franchises, Hematology, Rare Tumors and Solid Tumors.
As Medical Advisor Rare Tumors Sweden you have local product related responsibilities and responibiliy to offer medical/scientific support within franchise Rare Tumors.
Medivir is expanding and is looking for a candidate for a newly created role as Director R&D Projects, who will lead development projects from CD-selection to late clinical phases.
Medivir is expanding and is looking for a candidate for a newly created role as Vice President Clinical R&D, who will lead and develop the clinical R&D operations.
Vi söker en Quality Assurance Head Nordic till ett läkemedelsföretag i Stockholmsområdet. Du kommer att ha ansvar för att QA-arbetet byggs upp för att motsvara de krav som finns globalt.
We are looking for a person who can successfully take responsibility for the assessment of project candidates and develop and lead complex Life Science projects towards commercial endpoints.
To an international insurance company
to an international insurance company