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
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.
IQVIA is focused on using data and science to help healthcare clients find better solutions for their patients. Individuals joining us are assured of a rewarding career in Life Sciences Consulting, with opportunities to address diverse
ProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in and Cambridge, Massachusetts, USA. At ProQR, we are on a mission to edit RNA, treat disease and change lives. A
QbD Group offers knowledge & tailored solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. Currently we are looking for Project Managers (PM) in Qualification &
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
Vacaturebeschrijving Klik hieronder op \Solliciteren\ om uw sollicitatie ter overweging in te dienen. Zorg ervoor dat uw cv up-to-date is en dat u eerst de functie-eisen heeft gelezen. Als barista bij EMA in Amsterdam zorg jij voor
Vacaturebeschrijving Zorg ervoor dat u het onderstaande overzicht en de vereisten voor deze vacature volledig leest. Ga aan de slag als Chef de Partie bij European Medicines Agency (EMA) in Amsterdam! Werk in een professionele keuken, bereid
The European Medicines Agency (EMA) is located in Amsterdam, the Netherlands. Serving a population of 500 million citizens, we promote and protect public and animal health in EU Member States, as well as the countries of the
ProQR Therapeutics in Leiden, NL is seeking a Clinical Operations Lead (full-time) to direct end-to-end management of outsourced clinical trials, ensuring data integrity and patient safety. Zorg ervoor dat u solliciteert met alle gevraagde informatie, zoals
Overview Our client operates in the biopharmaceutical field and focuses on advanced cell‑based therapies for patients with severe and complex diseases. The organization combines cutting‑edge science with large‑scale operations in a highly regulated environment. To support
Senior Quality Governance Lead (Operational) Heeft u wat nodig is om te slagen? De volgende informatie dient door alle kandidaten zorgvuldig gelezen te worden. Working mode: On-site Duration: 6 months Languages: English and Dutch The Senior
Details Working hours: 40 hours per week Contract duration: until 31 December 2026 (likely chance of extension) Responsibilities Creating, reviewing, and approving qualification protocols, executed protocol summary reports, and Requirements Traceability Matrices for equipment, utilities, facilities,