QA Validation Engineer

vor 3 Wochen


Lausanne, Schweiz Axepta SA Vollzeit

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



Branche: Pharma-Industrie

Funktion: Ingenieurwesen/Planung

Anstellungsart: Festanstellung




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