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V&V Lead

LocationEindhoven, - None Specified -
Business SectorMedical Device
Contact email
Job ref26561
Publishedabout 3 hours ago
Verification & Validation (V&V) Lead – Medical Devices
We’re currently partnering with one of our top MedTech clients to find an experienced V&V Lead who’s ready to take ownership of critical V&V activities for an innovative medical device solution. This role is central to ensuring product safety, performance, and regulatory compliance across the full product lifecycle.
Key Responsibilities
  • Lead and execute the V&V strategy across the full product lifecycle
  • Develop, review, and maintain V&V plans, test protocols, and acceptance criteria
  • Oversee verification and validation testing in line with regulatory requirements
  • Ensure complete and compliant V&V documentation and reporting
  • Drive risk-based V&V activities, including root cause analysis and CAPAs
  • Support regulatory submissions, audits, and inspections
Key Criteria
  • 5+ years of experience in Verification & Validation within the medical device industry
  • Strong hands-on knowledge of MDR, ISO 13485, IEC 60601, and IEC 62304
  • Proven experience in V&V planning, execution, and documentation
  • Solid understanding of risk management, FMEA, and design control processes
What’s on Offer
  • Competitive salary and benefits package
  • Collaborative, multidisciplinary MedTech environment
  • High-ownership role with real influence on product quality
If this sounds like something you’d like to explore, feel free to reach out directly for a chat.
?f.signorello@panda-int.com
? +31 (0)20 20 44 502