About this role
Executive - Quality Control
Shalina Healthcare is a market leader in making quality healthcare products affordable and available across Africa. We achieve this by sourcing from WHO-approved production facilities in India and China and by focusing on our first-class distribution expertise.
Shalina Healthcare is privately owned and part of the Shalina Group. We have been operating in...
Executive - Quality Control
- Job Type Full Time
- Qualification BA/BSc/HND
- Experience 5 - 8 years
- Location Ogun
- Job Field Science
Job Purpose
- To ensure that all raw materials, in-process products, and finished pharmaceutical products meet the required quality standards in compliance with regulatory guidelines, GMP requirements, and company quality policies.
Key Responsibilities
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Perform routine and non-routine analysis of raw materials, in-process samples, finished products, and stability samples.
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Ensure compliance with Good Manufacturing Practices (GMP), GLP, and regulatory requirements (e.g., NAFDAC, WHO, FDA where applicable).
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Conduct chemical, physical, and instrumental analysis using equipment such as HPLC, GC, UV Spectrophotometer, and dissolution apparatus.
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Review and interpret analytical data and ensure accurate documentation of results.
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Prepare and standardize reagents, solutions, and volumetric standards.
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Maintain laboratory instruments and ensure calibration and validation are carried out as per schedule.
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Participate in method validation, method transfer, and verification activities.
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Investigate Out of Specification (OOS), Out of Trend (OOT), and deviations, and support root cause analysis and CAPA implementation.
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Ensure proper documentation in line with data integrity principles (ALCOA+).
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Maintain laboratory cleanliness and adhere to safety procedures.
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Support internal and external audits, including regulatory inspections.
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Prepare Certificates of Analysis (CoA) and ensure timely release of materials/products.
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Qualifications & Experience
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Bachelor’s Degree in Chemistry, Biochemistry, or related field.
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5–8 years’ experience in a pharmaceutical manufacturing environment.
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Strong knowledge of analytical techniques and laboratory instruments.
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Good understanding of GMP, GLP, and regulatory requirements (NAFDAC, WHO).