Company: Chemo-Pharma Laboratories
Location: Lagos
Job Type: Full Time
Apply Before: 2026-09-01
Job Description
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.
How to Apply
Interested and qualified candidates should send their Resume to: hr@chemopharmalabs.com and copy info@chemopharmalabs.com using the Job Title as the subject of the mail.
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Source: MyJobMag