Routine sampling and testing of Raw Materials (RM), Packaging Materials (PM), In-process samples, Finished Products (FP), stability samples, water samples and other samples and will support instrument operation, Qualification, calibration, documentation and product release activities to ensure uninterrupted QC operation.

Supervise laboratory investigations related to Out-of-Specification (OOs), Out-of-Trend (OOT), deviations laboratory incidents and CAPA implementation.

Ensure compliance with WHO GMP, PIC/S GMP, EU GMP, USP, BP, EP and applicable regulatory guidelines.

Maintain Good Documentation Practices (GDP), ALCOA+ data integrity principles and electronic/physical laboratory records.

Responsible to carry out any other duties as when assigned by Head of the Department.