Type of contract: Permanent contract
Mission: You are in charge of the quality compliance of processes and hardware and / or software systems used for the research or manufacturing of health products.
In particular, you must develop the validation strategy for computerized systems and carry out validation activities at the production site and / or operator.
You write and keep track of documents related to validation processes (protocols, procedures, reports, etc.).
Master’s Degree in Engineer, you have a first experience with on site of production and or operator in validation of computerized systems.
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