About the job

You will support our clients across the full medical device regulatory lifecycle.

Responsibilities

  • Maintain technical documentation to MDR standards.
  • Support internal and external audits.
  • Manage CAPA and non-conformance records.

Profile

  • Degree in life sciences or engineering.
  • 3+ years in a RAQA role.
  • Fluent English and French.

Workday Id

REQ-10483

Name

RAQA Specialist for Medical Devices

Publish Date

01 September, 2026

Start Date

2026-10-15

Spontaneous Application

RAQA Specialist for Medical Devices

New opportunities open up across PLG all the time. If nothing matches right now, send us a spontaneous application: we will keep you in mind for what comes next.

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