| Work location: | Switzerland, Vaud, lausanne |
| Sector: | Pharmaceutical |
| Role: | Engineering |
| Date of last update: | 09/04/2024 2024-07-09 |
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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 of contract: | Permanent job |
