Quality Assurance Manager

4 weken geleden


Almere, Flevoland, Nederland Panda International Voltijd

I'm working exclusively with a MedTech client in the Netherlands that is looking for an Interim Quality Manager to lead the Quality department, ensuring compliance with medical device regulations and maintaining operational excellence. This is a 6-month contract starting in Feb/March, with potential for extension.

Location: 100% On-site in Almere, Netherlands

Duration: Initial 6-month contract (possibility to extend)

Start Date: Feb/March

Interview Process: 1-stage Teams interview next week with an offer the same day

Responsibilities:

  • Oversee Quality Assurance and Document Control teams, ensuring compliance with ISO 13485, EU MDR, and GMP
  • Lead CAPA, non-conformance investigations, and complaint handling, implementing corrective actions
  • Manage QMS (Quality Management System), training records, and internal/external audits
  • Ensure the successful preparation and completion of regulatory inspections
  • Act as Management Representative for ISO 13485 compliance
  • Drive continuous improvement initiatives and ensure quality performance metrics are met
  • Support change controls, process validations, and risk management

Who We're Looking For:

  • 5+ years of Quality Assurance experience in medical devices
  • Strong knowledge of ISO 13485, EU MDR, GMP, and CAPA processes
  • Experience leading quality teams and working cross-functionally with regulatory, manufacturing, and engineering teams
  • Hands-on experience with document control, audits, and QMS maintenance
  • Strong problem-solving, stakeholder management, and leadership skills
  • Fluent in English (Dutch is a plus)

This is a fantastic opportunity to step into a leadership role at a growing MedTech company, driving quality excellence and compliance. Interested? Send your CV to c.girdwood@panda-int.com to discuss further


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