| Lieu de travail: | Suisse, Vaud, lausanne |
| Secteur: | Pharmaceutique |
| Poste: | Ingénierie/Planification |
| Date de la dernière mise à jour: | 09/04/2024 2024-07-09 |
Vérifiez votre compatibilité avec cette offre d'emploi
Our client, a medical devices company and one of the leaders in its field, is currently looking for a QA Validation Engineer.
YOUR RESPONSIBILITIES:
- Support qualification and validation activities in compliance with FDA and GMP requirements (production equipment)
- Participate in the review of technical and quality documentation for all departments (manufacturing, laboratory, etc.).
- Manage all documentation relating to manufacturing processes.
- Manage validation plans, risk analysis and statistics.
- Participate in the company's validation strategy and projects.
YOUR PROFILE :
- Master's degree in Lifescience with at least 5 years' experience in a similar position in a pharmaceutical or medical device company
- Good knowledge of qualification and validation, particularly on the process side.
- Good knowledge of statistics would be a real plus.
- Mastery of GMP and ISO 13 485 standards.
- Fluency in French and English.
For information adrien.menard@axepta.com
| Type de contrat: | CDI |
