Medtronic Benelux seeks an Associate Regulatory Affairs Specialist to support post‑market surveillance and quality management across Belgium, the Netherlands, and Luxembourg. The role collaborates with regulatory, quality and commercial teams to ensure patient safety and regulatory compliance. Based in Maastricht or Heerlen with a flex work arrangement, you will engage with authorities and customers, handle inquiries, and help implement new regulatory requirements across the Benelux region.
#J-18808-Ljbffr
Contactgegevens:
Recruitmentteam van NLS Medtronic Trading NL B.V.
