Brabant Wallon – Contracting As a QA Release Specialist, you will develop, assure and maintain the quality of the product and processes: Standard procedures Quality audits/review Raises and maintains the status of quality in the organisation. Enables a company to promote itself as one that provides quality goods and service. Involves Total Quality Management (TQM) programmes and the development of standard procedures in accordance with the company standards and cGMP Regulations. Ensures the release of products and raw materials in compliance with Good Manufacturing Practices, with the marketing authorization and regulatory requirements Manages and reviews Quality Reviews. Ensures and prepares the release of batches for the official control laboratories in a timely manner. Ensures timely escalation of quality issues, manages and reviews deviations, complaints, change controls in a timely manner University degree in sciences: Pharmacist, Bio Engineer, Biologist, Chemist Professional experience in a GMP Environment related to pharmaceutical production. Knowledge in deviation, CAPA, change control is preferred Fluent in written English, fluent in French Expertise recognized in several fields related to release system. Jefferson Wells offers you a permanent contra... Raw material, Universities, Expertise, Quality audit, VOS, GMP, Quality Reviews, Science, cGMP, GMP, Write English, Service, Laboratory Work, Change Control, French language, Quality assurance, Marketing, CAPA, Development, Regulation Originele vacature is te vinden op StepStone.be – Maak nu een Jobagent aan op StepStone en vind je droombaan! https://bit.ly/2jPYsZC Vind gelijkaardige jobs, informatie over werkgevers en carrièretips op StepStone.be!
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