Manufacturing

Documentation/compliance Officer

Chemo-Pharma Laboratories·Lagos, nigeria·Full Time·Internship
ManufacturingFull TimeInternship
-Closes Oct 31, 2026

Key Responsibilities

  • Prepare, review, update, and maintain Standard Operating Procedures (SOPs) and other quality documents
  • Control, file, and archive records, ensuring documents are accurate and easy to retrieve
  • Ensure company operations comply with NAFDAC regulations, Good Manufacturing Practice (GMP), and internal quality standards
  • Support internal audits and regulatory inspections by preparing and presenting required documentation
  • Track document revisions and make sure only current versions are in use
  • Work with production, quality, and other departments to keep documentation up to date

Requirements

  • A Bachelor's degree or HND in Pharmacy, Chemistry, or a related science field
  • A minimum of 3 years' experience in the pharmaceutical field
  • Proven experience writing, reviewing, and implementing SOPs
  • Good knowledge of NAFDAC regulations and Good Manufacturing Practice (GMP)
  • Strong attention to detail and good organizational skills
  • Excellent written and verbal communication skills
  • Proficiency in Microsoft Office applications

Key skills

BA/BSc/HND
Apply Now
Send your CV along with a cover letter tohr@chemopharmalabs.com

Please use the job title as the subject line of your email.

At a glance

Company

Chemo-Pharma Laboratories

Location

Lagos, nigeria

Employment

Full Time

Work style

Internship

Experience

Valid until

October 31, 2026

Created

October 15, 2026