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 Antwerp at pharma, biotech and CDMO sites, technically screened by a GMP consultant. There are currently 0 open roles in Antwerp 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 Antwerp and the Kempen: global pharma sites in Beerse and Geel, vaccine and biologics plants, port-based API manufacturing and one of Europe's largest pharma logistics hubs. 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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Register / upload CVConsultant for this discipline
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.
Yes, Flanders, with a focus on Antwerp, the Kempen (Beerse, Geel) and Ghent. Same technical screening, same consultant.
Gross is similar; Belgian packages add company car, meal vouchers, group insurance and a 13th month, so net comparisons need the whole package. Our salary guide shows both.