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
Apply for this role
Closes Saturday 31 October · 8 days left
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Documentation and Compliance Officer - Chemo-Pharma Laboratories
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