Quality Documentation & Compliance Lead (Medical Devices)

embecta is seeking a detail-oriented quality professional to manage batch records, drive document revisions, and maintain site documentation systems in a regulated manufacturing setting. You will work cross-functionally to support compliance, product release, and audit readiness.

The role requires a science or engineering qualification and at least 2 years in Medical Devices or Pharmaceutical manufacturing, with experience in SAP or similar QMS systems and a strong attention to detail.