Qualifications

• 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.

Knowledge and exposure to various analytical QC methods and equipment.

• 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.