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.
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
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
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
Are you someone who naturally sees how things can be organized better, documented more clearly, and executed more efficiently? Do you enjoy creating order, defining standards, and continuously improving the way work gets done? At Avantor,