Role DescriptionIn this role you will be responsible for the development and standardization of the quality management system and you will also be responsible for the communication between sub contractors and you will also be responsible for educating your fellow colleagues in GMP guidelines.
ResponsibilitiesEnsures that pharmaceutical sites are "inspection readiness" at all times Ensures the maintenance of the certifications of the quality management system Represents quality during audits of authorities
Coordinate and ensure internal audits for GxP activities at the various sites. Accompany auditors during external audits Provide support to the operational teams for the analysis of nonconformities according to the methods defined thus the correct follow-up of the corrective / preventive actions. Provide support for the qualitative assessment of subcontractors Quality performance analysis
RequirementsFluent in both written and English A master in a relevant education (pharmacy, life sciences) Excellent communication skills At least 3-5 years of experience in a similar role Excellent knowledge of Quality Management Systems
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