CSV Specialist Pharma (Junior) | (Junior) CSV Specialist Pharma (m/w/d)

Job Summary

This role involves executing Computerized System Validation (CSV) and qualification projects for various systems like MES, LIMS, PLS, and automated production facilities within the pharmaceutical industry. The specialist will be responsible for creating system life-cycle documents such as validation and qualification plans, requirement specifications, risk analyses, and test plans. Key responsibilities also include conducting and overseeing qualification measures (DQ, IQ, OQ, PQ), performing GAP analyses against pharmaceutical quality requirements, and advising clients on IT validation concepts. This position offers an opportunity to work on exciting projects with innovative companies, contribute ideas, and benefit from extensive training programs, making it an attractive option for professionals looking to advance their careers in pharmaceutical validation.