GMP QA: Batch Release & Certification Lead (On-site NL)

Cytiva; Medemblik; On-site; EUR 40,000 - 55,000; Full time

Job summary

Cytiva in Medemblik, Netherlands, is seeking a QA Batch Release Officer to review batch records and certify products for release. The role focuses on ensuring GMP-compliant documentation and final product release, within the on-site Quality Assurance team.

You will engage with non-conformance/rework actions and support routine QA tasks, contributing to safe, effective medicines and therapies. Collaboration with cross-functional teams is essential.

Qualifications

• Junior Bachelor’s degree / MBO in Life Sciences or related field.
• 1–3 years in quality and/or production environments.
• Team player with strong communication and attention to detail.

Responsibilities

• Review batch documentation to ensure GMP-compliant release.
• Certify finished goods for release to customers.
• Review customer documents for GMP compliance.

Skills

Team player

Attention to detail

Communication skills

Education

Bachelor’s degree / MBO in Life Sciences

Tools

GMP knowledge

Job description

Cytiva in Medemblik, Netherlands, is seeking a QA Batch Release Officer to review batch records and certify products for release. The role focuses on ensuring GMP-compliant documentation and final product release, within the on-site Quality Assurance team.

You will engage with non-conformance/rework actions and support routine QA tasks, contributing to safe, effective medicines and therapies. Collaboration with cross-functional teams is essential.