Quality Specialist

The Company: Our client is a global pharmaceutical organization specializing in specialty medicines and OTC products. The organization operates GMP-regulated manufacturing facilities and focuses on quality, patient safety, automation, and operational excellence.

Role Description: As a Quality Specialist, you will support GMP compliance and quality processes within a pharmaceutical manufacturing environment. You will work closely with Quality, Production, Engineering, and other teams to maintain high quality standards.

Responsibilities: Manage and support deviations, CAPA, and change controls. Support investigations and implement corrective actions. Review quality and manufacturing documentation. Support internal and external audits and inspections. Monitor GMP compliance and quality performance. Work with cross-functional teams to resolve quality issues. Support continuous improvement and quality initiatives. Promote a strong GMP and quality culture.

Requirements: Bachelor's degree in Life Sciences, Pharmacy, Chemistry, or a related field. Experience in QA/QC within a GMP pharmaceutical environment. Strong knowledge of GMP and quality systems. Experience with deviations, CAPA, and change control. Experience supporting audits and investigations. Strong communication, documentation, and analytical skills. Structured and detail-oriented approach. Experience in sterile, oncology, or OTC manufacturing is an advantage.

Dutch proficiency is strongly preferred.

Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.