We are seeking a QA Engineer Operational to join our team and play a key role in guaranteeing compliance with European and American GMP guidelines, ensuring the highest standards of pharmaceutical product quality.
Key Responsibilities:
* Review batch records and prepare release documentation
* Assess deviations, OOS/OOL, and vendor complaints
* Monitor and approve quality-related procedures, protocols, and reports
* Perform GxP shopfloor checks and support process improvements
* Lead risk analyses and implement CAPAs
* Oversee change control and quality-related projects
* Promote quality awareness, provide training, and drive continuous improvement
Your Profile:
* Master’s degree in Chemistry, Industrial Pharmacy, Biotechnology, Biomedical Sciences, or similar (or equivalent experience)
* Minimum of 2 years’ experience in a similar role within pharma, biotech, or medical devices
* Strong knowledge of GMP, GXP (EU & US) and quality systems
* Skilled in MS Office; SAP/MasterControl experience is an advantage
* Fluent in English, with good knowledge of Dutch and/or French (both is a strong asset)