Validation Engineer

Job Summary: The incumbent will independently lead validation activities for assigned equipment, processes, and computerized systems within a pharmaceutical facility. Responsibilities: ·      Develop and execute validation protocols(IQ/OQ/PQ, process validation, cleaning validation) and author final reports ·      Lead validation risk assessments and ensurecompliance with GMP/GAMP requirements ·      Investigate validation-related deviations andsupport CAPA implementation ·      Coordinate validation activities withcross-functional teams (QA, Engineering, Manufacturing) ·      Maintain and update validation master plans Requirements: ·      Degree in Engineering, Life Sciences, or related field ·      At least 4 to 7 years of validation experience in pharmaceutical/biotech manufacturing Contract: 12 months, subject to renewal based on performance