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,
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.
At Bynder, we don’t just store creative assets; we enable brands to deliver exceptional content experiences that drive business impact. Voordat u op deze functie solliciteert, verzoeken wij u de volgende informatie over deze vacature hieronder
#LI-Onsite Wilt u solliciteren? Zorg ervoor dat uw cv up-to-date is en lees vervolgens de volgende functiespecificaties zorgvuldig door voordat u solliciteert. Location: Baarle-Nassau, Netherlands As a Process Specialist, you will contribute to the manufacturing of
Imagine this You are the person who ensures every spare part, every serial number, and every logistics record is exactly where it needs to be, keeping our products mission ready throughout their entire lifecycle. As a Supply
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