QA Release Specialist
Brabant Wallon – Contracting
Your responsibilities?
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
Your profile?
- 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.
Our offer?
Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply or send me your CV, [email protected]
