Job Description De functie Als Biotech Specialist Downstream Processing (Associate Specialist Engineering) word je de procesexpert achter onze biologics-productie: Ben jij een biotechnoloog die energie krijgt van de shopfloor, van uitzoeken waarom een proces zich anders
The Document Control Engineer will be responsible for overseeing the lifecycle of quality‑related documentation related to product certificates, test reports, Manufacturing Record Books, type‑approval submissions, and ensuring that all documents meet internal standards and external regulatory requirements.
Salary Range:37.200,00 € - 69.000,00 € BandLevel 2 Job Description Summary#LI-Onsite Location: Baarle-Nassau , Netherlands A junior manufacturing technician contributes to the manufacturing of radiopharmaceutical products, at Novartis in Baarle-Nassau, according to the Standard Operating Procedures,
A commercial product. A new cleanroom. A scaling team. Lees de informatie in deze vacature zorgvuldig door om precies te begrijpen wat er van potentiële kandidaten wordt verwacht. Xeltis is scaling up commercial manufacturing of its
Orion Group Life Sciences are looking for a Senior Associate QA (GMP) (Validation / Packaging / PASX master data) for our Multinational Pharmaceutical/Biotechnology client based in Breda. Initial 12-month contract, with a high possibility of extension.
Wil jij aan de slag als operator en werken aan medicijnen die levens redden? Ben je nauwkeurig, kwaliteitsgericht en vind je het prettig om in de dagdienst te werken? Dan is deze baan in Oss perfect
This role is open for candidates across the EU with a valid passport who are willing to relocate to the south of The Netherlands for this opportunity. Controleer hieronder of u heeft wat nodig is voor
Work ScheduleOther Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed Job Description As part of the Thermo Fisher Scientific