Computer System Validation (CSV) Specialist/Engineer
About this role
About the Role We are seeking highly skilled technical professionals capable of providing commissioning and qualification services within the Pharmaceuticals, Biotechnology, and Medical Devices Manufacturing industries. The Computer System Validation (CSV) Specialist/Engineer will play a crucial role in the development and execution of software and equipment qualification processes. What You'll Do
- Generate and execute validation documents, including protocol creation and testing within the bio-pharmaceutical industry.
- Create and seek approval for validation documents such as C&Q Plan, URS, Design Specs, Requirements Traceability Matrix, and Summary Reports tailored for the Biopharmaceutical industry.
- Revise Design Specifications as necessary to align with new design requirements.
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