Selection procedure reference: EMA/TR/11539 Deadline for applications: 30 September 2026 23:59 CEST The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU), located in Amsterdam. It began operating in 1995. It is responsible for
Selection procedure reference: EMA/TR/11532 Deadline for applications: 30 September 2026 23:59 CEST The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU), located in Amsterdam. It began operating in 1995. It is responsible for
Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of
We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs
Selection procedure reference: EMA/TR/11542 Deadline for applications: 30 September 2026 23:59 CEST The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU), located in Amsterdam. It began operating in 1995. It is responsible for
Selection procedure reference: EMA/TR/11533 Deadline for applications: 30 September 2026 23:59 CEST The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU), located in Amsterdam. It began operating in 1995. It is responsible for
Selection procedure reference: EMA/TR/11538 Deadline for applications: 30 September 2026 23:59 CEST The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU), located in Amsterdam. It began operating in 1995. It is responsible for
Selection procedure reference: EMA/TR/11543 Deadline for applications: 30 September 2026 23:59 CEST The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU), located in Amsterdam. It began operating in 1995. It is responsible for
Selection procedure reference: EMA/TR/11545 Deadline for applications: 30 September 2026 23:59 CEST The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU), located in Amsterdam. It began operating in 1995. It is responsible for
Job grade: FGIV Internal/inter-agency job grade: FGIV Type of position: Contract agent Selection procedure reference: EMA/CA/11523 Job title: Transparency Officer Talent Pool: FGIV Science and Regulation Deadline for applications: 06 September 2026 at 23:59 CEST Salary: 4249,97
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Als (Senior) Equipment Engineer zorg je ervoor dat productieapparatuur technisch betrouwbaar én compliant functioneert binnen een GMP-omgeving. Je bent betrokken bij het volledige lifecycle-proces van equipment: van kwalificatie en ingebruikname tot optimalisatie en doorontwikkeling. Je werkt
Our client is an international biopharmaceutical organization focused on developing and bringing to market novel treatments for rare and ultra-rare genetic and immunological conditions. The company is patient-driven at its core, pairing strong scientific capability with
Who we are For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance
Avertim Netherlands is currently looking for Non-Conformities Specialists able to assist in the continuous expansion of Avertim’s consulting activities in Life Sciences. Located in Amsterdam-Zuid, Avertim Netherlands is a trusted partner of the largest players in
SENIOR MICROBIOLOGISCH ANALIST Ben jij een ervaren microbiologisch analist die graag verder kijkt dan alleen het uitvoeren van analyses? Krijg jij energie van het beoordelen van resultaten, het oplossen van microbiologische vraagstukken én het delen van
For our client, a global biopharmaceutical manufacturer recognised for its leadership in large molecule medicines, were looking to recruit a Director Quality Control to lead and elevate the Quality Control organisation supporting a complex biologics manufacturing
Engineer MSAT Validation – Biotherapeutics Drug Substance Responsible for supporting validation activities for biotherapeutic drug substance manufacturing within a GMP-regulated biotechnology environment. The role focuses on planning, coordinating, and executing Supporting Process Validation (SPV) activities to
About Us At Xe, we live currencies. We believe that behind every currency exchange, query or transaction is a person or business trying to accomplish something important. We work together to develop new and better currency
Ga aan de slag als chef de partie bij European Medicines Agency (EMA) in Amsterdam! Werk in een professionele keuken, bereid verfijnde gerechten en til samen met het team de culinaire beleving naar een hoger niveau. Klaar