Quality Business Partner - Medtech

Uniphar

3+ years medical devices or pharma distribution experience
Strong working knowledge of iso 13485 and mdr requirements
Experience with qms processes, audits, capa, and deviations
Act as a Quality subject matter expert across all MedTech teams and serve as the primary point of contact for EU Medtech business quality matters

Job Summary

  • Act as a Quality subject matter expert across all MedTech teams and serve as the primary point of contact for EU Medtech business quality matters.
  • Provide proactive quality input into new business models while ensuring rapid communication of risks and potential misconduct to leadership.
  • Support audit readiness, manage deviation investigations, and guide the team on MDR and supplier oversight requirements.

Matching Summary

Act as a Quality subject matter expert across all MedTech teams and serve as the primary point of contact for EU Medtech business quality matters.

Skills & Requirements

Must-have

  • 3+ years Medical Devices or Pharma distribution experience
  • Strong working knowledge of ISO 13485 and MDR requirements
  • Experience with QMS processes, audits, CAPA, and deviations
  • Expertise in supplier management and intercompany agreements
  • Ability to drive continuous improvement initiatives

Nice-to-have

  • Excellent communication and influencing skills
  • Strong analytical and problem-solving abilities
  • Proactive quality culture mindset
  • Cross-functional stakeholder engagement capabilities

Key Requirements

  • Minimum 3 years' experience in Medical Devices, MedTech, or Pharma distribution
  • Clean driver's license and ability to travel domestically and in Europe
  • Strong working knowledge of WDA distribution regulations

Work Rights

Not specified

Tailored Resume

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