RAPermanentDutch not required
Regulatory Affairs Officer – EU
Marketing authorisation holder, Amsterdam
Own 30 products across DCP/MRP; hybrid 2 days on site near the Zuidas.
€58–70k
Hybrid · Amsterdam
1 vacancy
Regulatory Affairs jobs
Regulatory Affairs jobs at pharma, biotech and CDMO sites, technically screened by a GMP consultant. There is currently 1 open role across the EU. Regulatory Affairs Officers, CMC Regulatory Specialists and RA Managers for EU submissions, variations, lifecycle maintenance and CMC dossiers. 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.
(Example vacancies. These show how a role is presented; they are not live searches.)
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
Regulatory Affairs jobs by city
Frequently asked questions
Do I need a pharmacy degree for Regulatory Affairs?
It helps but is not required. Life sciences, chemistry and QA or QC backgrounds are common entry routes, particularly into CMC-focused roles.
What is the difference between RA and QA?
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.
Can RA work be done remotely?
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.