Quality Control Officer at Shalina Healthcare

Job Purpose:

• To ensure that all raw materials, in-process materials, and finished products are tested according to approved specifications and meet quality standards, ensuring compliance with GMP, regulatory requirements, and company policies.

Key Responsibilities:

• Perform physical, chemical, and instrumental analysis of raw materials, packaging materials, in-process, and finished products.
• Ensure sampling, testing, and release are conducted in accordance with SOPs and cGMP requirements.
• Prepare and review test reports, COAs, and maintain accurate documentation.
• Calibrate and operate laboratory instruments such as HPLC, UV-Vis Spectrophotometer, FTIR, pH meter, etc.
• Participate in method validation, method transfer, and stability studies.
• Conduct environmental and water testing as required.
• Report and investigate OOS (Out of Specification) and OOT (Out of Trend) results.
• Maintain laboratory cleanliness and ensure safety practices are followed.
• Support internal and external audits and implement corrective/preventive actions (CAPAs).
• Collaborate with Production, QA, and other departments to resolve quality-related issues.

Qualifications and Experience:

• B.Sc. or HND in Chemistry, Biochemistry, Microbiology, or related sciences.
• 2–5 years of relevant QC experience in a pharmaceutical manufacturing environment.
• Good knowledge of cGMP, GLP, and regulatory guidelines (e.g., NAFDAC, WHO, FDA).
• Experience with analytical instruments like HPLC, UV, FTIR, etc.

Key Skills and Competencies:

• Attention to detail and accuracy.
• Strong analytical and problem-solving skills.
• Good documentation and communication skills.
• Proficiency in Microsoft Office tools.
• Ability to work independently and as part of a team.
• Time management and ability to handle multiple tasks.