Chemo-Pharma Laboratories Ltd. was established in 1985.The Company has an Installed Capacity of 6.0million bottles of liquid syrup and 310.2 million tablets per annum respectively. This installed capacity has for sometime now become inadequate to cater for expected growth. It has strained working capital and created excessive overheads. Also the company runs a well equipped Quality Assurance Laboratory.

We are recruiting to fill the position below:

Job Title: Documentation / Compliance Officer

Location: Oregun, Lagos
Employment Type: Full-time

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.