Chemo-Pharma Laboratories Ltd.
Pharmaceuticals & Biotechnology
Documentation / Compliance Officer
About this role
Chemo-Pharma Laboratories Ltd.—a pharmaceutical manufacturing enterprise with a production capacity exceeding 300 million units per annum—is recruiting a Documentation / Compliance Officer for its plant in Oregun, Lagos State. This quality assurance and regulatory affairs role manages Good Manufacturing Practice (GMP) document control, NAFDAC regulatory compliance, internal quality audits, batch record archiving, and Corrective and Preventive Action (CAPA) tracking.
Key Responsibilities
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Document Control & Standard Operating Procedures (SOPs): Author, review, update, and archive SOPs, batch production records, analytical specifications, and quality manuals.
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Regulatory Compliance & Audits: Ensure manufacturing operations comply with NAFDAC and WHO-GMP standards; organize internal audits and lead preparations for external regulatory inspections.
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Deviation Management & CAPA: Investigate quality deviations, log non-conformances, track CAPA implementations, and verify corrective action efficacy.
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Staff Training: Conduct regular training sessions for production and quality personnel regarding GMP guidelines and document compliance workflows.
Requirements & Qualifications
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Academic Background: Bachelor’s Degree in Pharmacy (B.Pharm), Industrial Chemistry, Microbiology, Biochemistry, or a related scientific discipline.
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Work Experience: Over 5 years of practical QA/regulatory compliance experience within pharmaceutical or allied manufacturing settings.
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Core Competencies: Deep knowledge of NAFDAC regulations, WHO-GMP guidelines, technical writing, audit readiness, and attention to detail.
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