(Junior) Computer System Validation (CSV) Specialist Pharma | (Junior) CSV Specialist Pharma (m/w/d)

Job Summary

As a (Junior) CSV Specialist in the pharmaceutical sector, you will be responsible for executing computer system validation and qualification projects for critical systems such as MES, LIMS, and automated production plants. Your daily tasks involve creating essential System Life Cycle documentation, including validation plans, risk analyses, and test protocols (DQ, IQ, OQ, PQ). You will perform GAP analyses against pharmaceutical quality standards and advise clients on IT validation concepts. This role offers a unique opportunity to work on diverse projects for innovative companies while benefiting from a permanent contract, extensive professional development programs, and comprehensive benefits like pension schemes and childcare subsidies. It is an ideal position for those looking to bridge the gap between technology and life sciences within a supportive, growth-oriented environment.