Job Description

Job description



Mission Description


We are seeking a skilled and motivated Validation Engineer to join our team, supporting the validation of computerized systems within a cGMP-regulated pharmaceutical environment. The ideal candidate will ensure that all systems remain in a validated state throughout their lifecycle, in compliance with regulatory requirements (FDA, EU GMP, 21 CFR Part 11) and internal standards.


This role is hands-on and project-driven, with a focus on delivering robust validation documentation and execution for critical systems used in manufacturing, laboratory, and quality operations.


Key Accountabilities




  • Develop, implement, and execute User Requirement Specifications (URS), System Impact Assessment (SIA), Design Qualification ...

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