2026–present
Rijksen Regulatory House
Independent senior QA/RA consultant for Pharma, MedTech and other regulated organisations.
Over 25 years in QA/RA and life sciences.
From toxicology and regulatory assessment to GMP pharmaceutical manufacturing, government, healthcare materials and MedTech.
2025–2026
External QA/RA assignments
Support in pharmaceutical manufacturing and early-stage MedTech, including regulatory positioning, QMS set-up and technical documentation.
2017–2025
RENOLIT Nederland
Manager Regulatory Affairs for international healthcare materials, including product and material compliance and food-contact compliance.
2011–2017
MSD
Senior Quality Assurance in a GMP manufacturing environment, with QA responsibilities and process improvement.
2007–2011
TNO / Triskelion
Project management in toxicology, exposure assessment and European chemicals regulation.
2006–2007
CBG/MEB
Regulatory Project Manager for national and European medicinal product procedures.
1996–2006
RIVM, Elsevier en TEVA/Pharmachemie
Scientific assessment, publication processes and quality documentation in life sciences.
Not every challenge requires a large programme. In an initial conversation, we look at what is needed and whether my expertise is the right fit.