job description

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.

For agap2, all talents count. If you are disabled, do not hesitate to ask us your questions and to apply.