Skip to content

0 vacancies

Regulatory Affairs jobs in Eindhoven

Regulatory Affairs jobs in Eindhoven at pharma, biotech and CDMO sites, technically screened by a GMP consultant. There are currently 0 open roles in Eindhoven and the surrounding area. Regulatory Affairs Officers, CMC Regulatory Specialists and RA Managers for EU submissions, variations, lifecycle maintenance and CMC dossiers. GMP, ISO 13485 and MDR jobs in Eindhoven: Brainport's health-tech and medical device industry, combination products, sterile devices and the engineering firms that build pharma automation. 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.

No vacancies match these filters. Register and we will call you when one opens.

Register / upload CV

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

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.

Are there pharma GMP jobs in Eindhoven?

Mostly device, combination product and automation-related: ISO 13485 QA, MDR RA, process and computerised systems validation. Classical drug manufacturing is in Oss, Leiden and Bilthoven.

Is English enough in Eindhoven?

Yes at most Brainport companies, the region is one of the most international in the Netherlands.