Regulatory Affairs Manager at MeCure Healthcare, Lagos: A Senior Pharmacy Role in Nigerian Manufacturing

The MeCure Healthcare Regulatory Affairs Manager position offers an outstanding career path for pharmacists specializing in NAFDAC product registration dossiers, regulatory compliance, and Good Manufacturing Practice (GMP) standards.

MeCure Healthcare Regulatory Affairs Manager Vacancy Overview

Regulatory Affairs Manager (Lagos State, Nigeria)

• Organization: MeCure Healthcare Limited

• Location: Lagos State, Nigeria

• Role Overview: The MeCure Healthcare Regulatory Affairs Manager leads the assembly and submission of NAFDAC product registration dossiers, oversees product renewals and post-approval variations, maintains audit-ready GMP documentation, and serves as the primary technical interface between the company and regulatory bodies.

• Eligibility Criteria:

  • Bachelor of Pharmacy (B.Pharm) degree from a recognized institution.

  • Minimum of 3 to 5 years of progressive regulatory affairs experience within the pharmaceutical industry.

  • Demonstrated track record of preparing and managing end-to-end NAFDAC product registrations, renewals, and variations.

  • In-depth knowledge of local and international pharmaceutical regulations, including NAFDAC guidelines, GMP, and international standards.

  • Community or hospital pharmacists lacking industrial regulatory dossier experience do not qualify.

  • Non-pharmacy graduates are not eligible for this role.

• Compensation & Benefits: Undisclosed competitive industry package; full-time national contract.

• Deadline: Rolling / September 2026 (Posted August 26, 2026).

• How to Apply:

  • Submit your detailed CV directly to hr@mecure.com.ng.

  • Use the exact position title as the subject line: Regulatory Affairs Manager.

  • Application Tip: In your email opening paragraph, explicitly detail the total number of dossiers you have successfully submitted to NAFDAC, list specific product lines managed, and highlight any specialized experience with WHO prequalification, export registrations, or ECOWAS harmonization.

Strategic Career Insights

Regulatory affairs represents one of the most transferable and high-yield non-clinical specialties for African pharmacists. As local medicine manufacturing accelerates across West Africa to improve health security, pharmacists who can navigate multi-country registration pathways and complex regulatory audits become invaluable assets to pharmaceutical manufacturers.

Frequently Asked Questions

Are pharmacists from hospital or community settings eligible to apply?

Candidates must possess direct experience preparing industrial pharmaceutical product dossiers and running NAFDAC regulatory pathways. Hospital or community experience alone does not meet the eligibility requirements.

Is a Master’s degree or specialized certification required for this role?

A B.Pharm degree with 3–5 years of practical regulatory affairs experience is the stated requirement. While additional certifications are beneficial, verified experience taking dossiers to approval is the primary selection criteria.