Minimum Degree in Chemistry, Pharmacy, Lab technology, Microbiology or a related field.

At least three (3) years of experience in a laboratory in pharmaceutical manufacturing.

Strong knowledge of regulatory requirements pertaining to GMP and GLPs.

Conduct analysis of raw materials, finished products, stability, and validation samples in compliance with approved procedures and quality standards.

Receive, handle, and store laboratory samples while ensuring sample integrity throughout the analysis process.

Prepare and maintain test solutions, reagents, and volumetric solutions.

Operate, calibrate, and perform routine maintenance of QC laboratory instruments and equipment.

Prepare accurate analytical reports and maintain all laboratory records, registers, and documentation.

Support preparation and review of raw material, finished product, and stability specifications.

Update analysis status in manual and electronic data management systems.

Report deviations, unusual observations, or laboratory incidents promptly.

Ensure compliance with cGMP, GDocP, ALCOA principles, and company data integrity requirements.