Documentation / Compliance Officer at Chemo-Pharma Laboratories

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• • Documentation / Compliance Officer at Chemo-Pharma Laboratories
  • View Jobs in Healthcare / Medical / View Jobs at Chemo-Pharma Laboratories

  Posted: Aug 18, 2026

  Deadline: Not specified

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  We are a leading manufacturing pharmaceutical company whose major priority centers on the healthy well being of everyone. Our mission is to build a healthier tomorrow for patients , provision of health facilities for the creation of a healthy nation.

  
  

  Documentation / Compliance Officer

  • Job Type Full Time
  • Qualification BA/BSc/HND
  • Experience 5 years
  • Location Lagos
  • Job Field Pharmaceutical&nbsp

  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.

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  Method of Application

  Interested and qualified candidates should send their Resume to: [email protected] and copy [email protected] using the Job Title as the subject of the mail.

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