Gestion de Deviations Pharmaceuticals F/M/X - Brugge
1 maand geleden
Job summary
We are looking for a Deviation Management Specialist to lead the end-to-end management of deviations in compliance with GMP (Good Manufacturing Practice), ISO 13485, and EU Directive 2001/83/EC.This role involves investigating root causes, conducting impact assessments, and implementing corrective actions to prevent future deviations.
The ideal candidate will have a strong background in pharmaceutical quality assurance with experience in deviation management. They should be familiar with GMP-regulated environments and possess excellent analytical skills.
We are committed to providing our candidates with the best possible recruitment experience. If you are passionate about ensuring product quality and safety while working in a dynamic environment,
we encourage you to apply!
Functieomschrijving
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