Qualification and Validation Technician

Your mission: Qualification and Validation Technician Your mission: Writing of qualification protocols and reports Execution and documentation of qualification and metrology activities (initial and periodic) Coordination and control of the different qualification stages with the relevant departments Writing and execution of computerized system qualification protocols (URS, IQ, OQ, PQ) Control of the regulatory compliance of systems according to GMP, 21 CFR Part 11 and Annex 11 requirements Analysis of deviations, documentation of deviations and proposal of corrective and preventive actions (CAPA) Participation in the cleaning validation of production equipment in accordance with current regulations Your profile: Degree in the fields of qualification/validation, automation or equivalent Proven experience in qualification/validation of systems and processes in a GMP environment Indispensable experience in the pharmaceutical industry Good knowledge of GMP/BPF as well as 21 CFR Part 11 requirements Experience in CSV (Computer System Validation) Proficiency in French and English Autonomy, rigor, team spirit, sense of responsibility and ability to propose solutions What we offer: Individualized follow-up for the optimization of your CV and interview preparation. Opportunity within a renowned pharmaceutical company. Temporary mission with the possibility of extension according to the needs of the company. Interested? Do not hesitate to send us your complete file following the instructions below. Only files corresponding to our need will be processed jpid0eb3c7ejm jpit0834jm jpiy26jm