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