Job Description Do you have experience with medical devices, automation, and process validation in a regulated environment? Join an innovative team at one of the largest pharmaceutical manufacturing companies in the Netherlands. At our Haarlem site,
About the Role We are seeking an experienced Production Expert III to support pharmaceutical manufacturing operations within a highly regulated production environment. This is an excellent opportunity for a quality-focused professional to play a key role
Prothya Biosolutions is currently seeking a motivated and detail-oriented Senior QA Officer QMS to join our Quality Assurance team. In this role, you will play a key part in ensuring GMP compliance, supporting QP batch release
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
Preparation of QP batch release for Products (Quality records, Batch record review, release documentation), overall QMS compliance relating to QA Operational tasks. You play a key role in executing structured simple Root Cause Analyses (RCA), tracking
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,
Employment Type: Contract length N/A yet Scroll naar beneden voor een compleet overzicht van wat deze baan inhoudt. Bent u de juiste kandidaat voor deze functie? About the Company A growing international pharmaceutical organisation with a
Overview The Quality Control (QC) Senior Laboratory Technician - Chemistry plays a critical role in ensuring compliance of our pharmaceutical products and raw materials. As a QC Laboratory Senior Technician you are responsible for performing a
Overview Overview Solliciteer nu, lees de vacaturedetails door naar beneden te scrollen. Controleer of u over de nodige vaardigheden beschikt voordat u een sollicitatie verstuurt. Associate Director Global CMC QU – Clinical GMP/GDP at Kyowa Kirin
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our