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,
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 &
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,
UBIKK. zoekt een Medior / Senior Engineer! Solliciteer snel! Er wordt een groot aantal sollicitanten verwacht voor de hieronder beschreven functie, wacht niet met het versturen van uw cv. Heb jij ervaring met kwalificatie en validatie