Documentation/Compliance Officer at Chemo-Pharma Laboratories

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