Consultant for this discipline
Gregory Sivo
Founder · Practising GMP quality professional
- · Founder, Truex Consultancy: GMP and GDP compliance
- · 10+ years in regulated pharmaceutical quality
- · Personally conducts every technical conversation
0 vacancies
Regulatory Affairs jobs in Utrecht at pharma, biotech and CDMO sites, technically screened by a GMP consultant. There are currently 0 open roles in Utrecht and the surrounding area. Regulatory Affairs Officers, CMC Regulatory Specialists and RA Managers for EU submissions, variations, lifecycle maintenance and CMC dossiers. GMP jobs in Utrecht: generics manufacturers, MAH quality and regulatory teams, contract labs and the Utrecht Science Park's regenerative medicine cluster, central and commutable from everywhere. Salaries for Regulatory Affairs roles run from €50–78k gross per year across medior to senior profiles; interim day rates and regional differences are in our salary guide. Every vacancy states the client type, contract form, salary band and whether Dutch is required. Not seeing the right role? Register and we will call you when one opens; most Regulatory Affairs roles in this market are never advertised.
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Founder · Practising GMP quality professional
It helps but is not required. Life sciences, chemistry and QA or QC backgrounds are common entry routes, particularly into CMC-focused roles.
QA controls what the site does; RA controls what the authority has approved the site to do. The two must stay in step, and the best RA Officers have spent time in QA or on the floor.
Often partly. Dossier work is desk-based, but CMC roles need regular contact with the site and its data. We state the arrangement on every vacancy.
More often than in Leiden or Amsterdam. Generics manufacturing sites usually want B1–B2 Dutch for QA Officers; MAH regulatory and QP roles are mostly English.
Generics and OTC manufacturers, MAHs, GDP wholesalers, contract labs and ATMP research groups on the Utrecht Science Park.