About the Role
Sagar Vitaceuticals Nigeria Limited, a leading household name in the Nigerian healthcare and pharmaceutical industry renowned for trusted brands like Vitaclox and Vitacillin, is seeking a dedicated and detail-oriented Documentation Executive. In this vital role based at our ultra-modern Ikeja facility, you will oversee the creation, review, control, and archiving of critical pharmaceutical documents in strict compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
Key Responsibilities- Prepare, review, issue, revise, and archive controlled documents including Standard Operating Procedures (SOPs), Batch Manufacturing Records (BMRs), and specifications.
- Maintain a robust document control system to ensure only current, approved versions are accessible across departments.
- Ensure full compliance with GMP, GDP, and relevant regulatory standards such as NAFDAC, WHO, and FDA requirements.
- Coordinate seamlessly with Quality Assurance, Production, and Regulatory Affairs teams during internal, customer, and regulatory audits.
- Support change control, deviations, CAPA documentation, and conduct training on document control procedures.
- Bachelor's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Microbiology, Biochemistry, or a related life science discipline.
- 2 to 5 years of proven experience in pharmaceutical documentation, quality assurance, or manufacturing environments.
- Strong working knowledge of GMP, GDP, and electronic document management systems (EDMS).
- Exceptional attention to detail, strong proofreading abilities, and high proficiency in Microsoft Office applications.
- Competitive salary with attractive performance-based incentives.
- Comprehensive health insurance and medical benefits.
- Opportunities for professional career progression within a renowned pharmaceutical leader.
- Dynamic, collaborative work environment at our state-of-the-art facility in Lagos.