Regulatory Affairs Specialist
Support dossier preparation, product registration, and lifecycle variations across Nigeria and regional markets.
Role overview
Department: Regulatory
Location: Lagos, Nigeria
Type: Full-time
Level: Mid
Deadline: 2026-04-15
Responsibilities
- Prepare and review NAFDAC submissions for new and existing products.
- Coordinate responses to regulatory queries and inspection findings.
- Maintain regulatory documentation, trackers, and product licenses.
- Collaborate with QA, QC, and Manufacturing to ensure compliance readiness.
Requirements
- B.Pharm or related life science degree (M.Sc. is an advantage).
- 3+ years in regulatory affairs within pharma or FMCG (regulated).
- Strong writing, attention to detail, and stakeholder management.
Apply for this role