Nusantara Prime Consulting Pte. Ltd.
Singapore / Global
Singapore / Global
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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Singapore / Global
Singapore / Global
Singapore / Global
Singapore / Global
Singapore / Global
Singapore / Global