Senior Specialist Computer System Validation Engineer m/w/d

We are currently looking for someone for our longstanding customer, a manufacturing pharmaceutical company Senior Specialist Computer System Validation Engineer m/w/d Leading assigned Commissioning, Qualification and Validation (CQV) activities focusing on Computer System Validation (CSV). Subsystem owner (SSO) for CSV. Additionally support CQV activities for equipment, processes, and sterilizations. Development and approval of CQV Plans and Reports. Provide technical and CQV knowledge to equipment and systems owners including best practices and optimizations. Establish and/or participate in risk analysis and assessment to support CQV activities and change management Support Change Management, Deviation Management, and CAPA Management process on site and timely closure of tasks from the aforementioned Follow GMP, company, and local regulations regarding safety and CQV activities Works closely with IT, Automation, Quality, CQV, and Productions to ensure systems are compliant Support site CQV program by conducting periodic reviews, requalifications,

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