Regulatory Affairs Manager
AI summary
MeCure Healthcare Limited is hiring a Regulatory Affairs Manager in Lagos to lead all regulatory activities for its pharmaceutical manufacturing and diagnostic operations. The role involves managing product registrations, NAFDAC submissions, license renewals, regulatory inspections, and cross-functional compliance. Candidates need a Bachelor's in Pharmacy and 3–5 years of progressive regulatory affairs experience in the pharmaceutical industry.
- Pharmaceutical regulatory leadership role in Lagos
- Manage NAFDAC submissions, renewals, and inspections
- Bachelor's in Pharmacy required
- 3–5 years progressive regulatory affairs experience needed
- Collaborate with QA, Production, R&D, and Supply Chain teams
- Apply by emailing hr@mecure.com.ng
AI job guide
Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.
AI salary guide
Not enough public dataNot enough public salary data is available for this exact role. Before applying, prepare to ask about gross pay, benefits, contract length, probation period, transport and any allowances.
Can you qualify for this role?
- Required3+ years of relevant experienceThe job post includes a minimum experience signal.
- RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
- PreferredPractical evidence in internship, Regulatory Affairs, Pharmaceutical RegulatoryThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in Not specifiedThe vacancy is associated with this location.
- UnclearComfort with the Full Time contract termsConfirm hours, duration, probation and benefits at the original source.
Documents to prepare
- Likely requiredUpdated CV
- Role specificCover letter or short employer message
- OptionalProfessional references
- Role specificAcademic or professional certificates
- VerifyLicence, permit or professional registration
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Regulatory Affairs Manager evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to MeCure Healthcare Limited (MHL) and the role in Not specified.
- Add concrete examples related to internship, Regulatory Affairs, Pharmaceutical Regulatory, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from MyJobMag Nigeria; avoid sending documents to unofficial contacts or copied links.
- Confirm the deadline, interview location and employer contact before sharing personal documents.
- Prepare a polite question about pay, benefits and contract terms for later interview stages.
Source and safety check
- MyJobMag Nigeria
- Original source link available
- Application method is clear
- Deadline not specified
- No major risk signal was detected in the captured text.
Never pay for interviews, shortlisting, medical checks, uniforms, or job placement. Confirm every application at the original source before sharing personal documents. Report suspicious listing.
Interview preparation
- What experience makes you a strong fit for this Regulatory Affairs Manager role in internship, Regulatory Affairs?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Not specified under the listed contract or schedule?
- Prepare examples with clear responsibilities, tools used and measurable outcomes.
- Review the source and research MeCure Healthcare Limited (MHL) before the interview.
Ask what the first priorities will be in the role and how success will be measured.
Similar jobs to consider
Use AI to apply better
After confirming the original source, use Career Assistant to check role fit, tailor your CV and prepare a cover letter or employer message.
Original source description
Me Cure Services - Diagnostic & Healthcare Center Nigeria Me Cure Healthcare Limited (MHL) is a Leader in the Medical Diagnostic and Healthcare sector in Nigeria and the West African sub-region with an established Pharmaceutical Manufacturing Company in Lagos, and Diagnostic Centers in Lagos, Victoria Islands and Kano. Regulatory Affairs Manager Job Type Full Time Qualification BA/BSc/HND Experience: 3 - 5 years Location Lagos Job Field Pharmaceutical Job Role Overview The Regulatory Affairs Manager is responsible for managing all regulatory activities of the company to ensure compliance with applicable pharmaceutical regulations and requirements. The role involves coordinating product registrations, regulatory submissions, license renewals, regulatory inspections and maintaining effective communication with regulatory authorities to ensure continuous market authorization and compliance of pharmaceutical products. Major Responsibilities: Develop and implement regulatory strategies to support product registration, market authorization and business objectives. Prepare, review and submit regulatory dossiers, applications, variations and renewals to regulatory authorities, including National Agency for Food and Drug Administration and Control and other relevant agencies. Ensure timely registration, renewal and maintenance of product licenses, permits and certifications. Monitor and interpret changes in pharmaceutical regulations, guidelines, standards and ensure company compliance. Serve as the primary liaison between the company and regulatory authorities on regulatory matters. Coordinate and support regulatory inspections, audits and assessments, ensuring timely closure of observations and corrective actions. Review product labels, packaging materials, promotional materials and artwork to ensure regulatory compliance. Collaborate with Quality Assurance, Production, Research & Development, Pharmacovigilance and Supply Chain teams to ensure regulatory requirements: are met throughout the product lifecycle. Maintain accurate and up-to-date regulatory documentation, databases and records for all registered products. Evaluate and approve regulatory aspects of product changes, variations and post-approval commitments. Provide regulatory guidance and training to internal stakeholders on applicable regulations and compliance requirements. Monitor product registration timelines and ensure timely submission of required documentation to avoid regulatory delays. Review technical documents, product specifications, manufacturing information, and quality data for regulatory submissions. Ensure compliance with local and international pharmaceutical regulations, guidelines and Good Manufacturing Practices (GMP). Educational Requirement: Bachelor's in Pharmacy Other Requirements: Minimum of 3–5 years of progressive experience: in Regulatory Affairs within the pharmaceutical industry. Strong knowledge of pharmaceutical regulations, registration requirements: and guidelines, including NAFDAC regulations, GMP and other applicable international standards. Proven experience: in preparing and managing regulatory submissions, product registrations, renewals and variations. Thorough understanding of pharmaceutical product lifecycle management and regulatory compliance requirements. Strong attention to detail with the ability to review technical and regulatory documents accurately. Ability to work collaboratively with Quality Assurance, Production, Research & Development, Pharmacovigilance and Supply Chain teams. Strong report writing, presentation and documentation skills Check how your CV aligns with this job Method of Application Send a direct message or your application/resume to hr@mecure.com.ng Build your CV for free. Download in different templates.