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Documentation / Compliance Officer

Chemo-Pharma Labs Limited

Oregun, Lagos

Key Responsibilities

  • Regulatory Compliance: Ensure company operations follow NAFDAC regulations and global Good Manufacturing Practice (GMP) standards.
  • Document Control: Create, review, update, and archive Standard Operating Procedures (SOPs), batch records, and quality manuals
  • .Audit Management: Lead internal quality audits and prepare the facility for external NAFDAC inspections or regulatory audits.
  • Training Coordination: Train staff on compliance policies, document control systems, and current GMP guidelines.
  • Deviation & CAPA Tracking: Log quality deviations, manage investigations, and monitor Corrective and Preventive Actions (CAPAs).

Requirements and Qualifications

  • A Bachelor's Degree in Pharmacy (B.Pharm), Industrial Chemistry, Microbiology, Biochemistry, or a related science field.
  • More than 5 years of experience in quality assurance, regulatory affairs, or document control within a regulated manufacturing environment.
  • Skills: Strong knowledge of NAFDAC/WHO GMP guidelines, excellent attention to detail, strong technical writing skills, and good computer literacy.

Application Closing Date
26th September, 2026.

How to Apply
Interested and qualified candidates should send their Resume to: and copy using the Job Title as the subject of the mail.

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Vacancy posted 6 hours ago
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