Description de l'annonce:

Remote Work, you  monitor the validation plan, as well as the management of the validation management computer system, eVMP, and the management of validation documents, from the assignment of codes to their final file. 

You carry out the review of sterilization cycles and performs autoclave validation studies. Make all kinds of validation documents and collaborate in carrying out calibrations.

Technical professional degree or equivalent with experience, desirable training university in technical area (Engineering, chemistry, pharmacy, technical engineering, etc.). One-two years of experience in the area of production and/or maintenance and/or Quality in thepharmaceutical industry, preferably in the area of validations You are fluent in both english and french.