Skip to content
Back to jobs

Quality and Regulatory Affairs Specialist

  • Stryker
  • Maastricht, Netherlands, Netherlands
  • Hybrid
  • Posted

Source: Stryker’s own career site First seen

Open original posting (opens in a new tab)

About the job

Work Flexibility: Hybrid. Join the team dedicated to ensuring the safety, quality, and compliance of life-saving medical devices. In this role, you will contribute directly to post-market surveillance and vigilance activities, helping to protect patients while supporting global regulatory compliance.

This is a short extract. Read the full posting and apply on the employer’s site.

See how well you fit this job

Log in and we compare this role with your CV: where you are a strong fit, where you are not, and what is worth saying about the gaps. You can also prepare a CV and cover letter written for this role.