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Supervise QC laboratory operations and testing activities
Review and interpret in-process and finished product analytical results
Ensure compliance with GMP, GLP, and regulatory requirements
Identify quality trends, risks, and recurring laboratory issues
Approve or reject materials and products based on analytical outcomes
Audit and monitor manufacturing and QC processes for compliance
Review and approve analytical data, COAs, and laboratory documentation
Lead investigations of deviations, OOS/OOT, and non-conformances
Drive CAPA effectiveness and continuous improvement initiatives
Prepare teams for internal, external, and regulatory audits
Mentor, develop, and manage QC laboratory leadership teams
Additional Responsibilities:
Responsible for the operation & calibration of balances in Sampling room & to maintain its record.
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