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

Job Summary

As a Computer System Validation (CSV) Specialist in the pharmaceutical and life science sector, you will play a critical role in ensuring that complex automated systems and software meet rigorous industry standards. Your day-to-day responsibilities will involve managing the full system life cycle, including the creation of validation and qualification plans, user requirement specifications, and detailed risk analyses. You will conduct qualification measures (DQ, IQ, OQ, PQ) and perform gap analyses to ensure compliance with pharmaceutical quality requirements. Additionally, you will support IT change management, test management, and provide expert consultation to clients during the implementation of IT validation concepts. This role is ideal for a detail-oriented professional who thrives in a project-based environment and is eager to contribute to digital transformation. You will benefit from a permanent contract, continuous professional development opportunities, and exposure to innovative projects with renowned clients in the life science industry, all while being supported by a company that values individual engagement and technical expertise.