QA Officer – Sterile Fill/Finish
Sterile CDMO, Leiden Bio Science Park
Annex 1 upgrade project, RABS to isolator conversion, you own the QA side.
2 vacancies
Quality Assurance jobs at pharma, biotech and CDMO sites, technically screened by a GMP consultant. There are currently 2 open roles across the EU. QA Officers, QA Specialists and QA Managers for batch release, deviations, CAPA, change control and inspection readiness at GMP sites across the European Union. 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.
(Example vacancies. These show how a role is presented; they are not live searches.)
Sterile CDMO, Leiden Bio Science Park
Annex 1 upgrade project, RABS to isolator conversion, you own the QA side.
Cell therapy biotech, Tech Lane Ghent
Build the quality system for a first FAMHP GMP licence; Part IV ATMP.
Consultant 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.