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
Quality Assurance 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. QA Officers, QA Specialists and QA Managers for batch release, deviations, CAPA, change control and inspection readiness at GMP sites across the European Union. 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 Quality Assurance roles run from €52–75k 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 Quality Assurance roles in this market are never advertised.
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Register / upload CVConsultant for this discipline
Founder · Practising GMP quality professional
At most CDMOs, biotech and vaccine sites the quality system runs in English. Sites with a local-language shop floor usually want a working level of that language for QA Officers who review batch records with operators. We state the language requirement on every vacancy.
In practice the Specialist title marks a senior individual contributor who owns a system (deviations, change control, supplier qualification, validation QA) rather than a queue. It is the usual stepping stone to team lead.
Yes, and it is the most common route. Two to three years of QC with exposure to OOS investigations and method validation is enough for most QA Officer roles.
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.