- Islandwide (Singapore) Singapore

Working Location
Job Description
Responsibilities
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
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