Assistant Manager, Regulatory Affairs
AI summary
Zamiva Transnational Services is hiring an Assistant Manager, Regulatory Affairs to lead pharmaceutical product registration, dossier management, and regulatory authority liaison in Nigeria. The role focuses on NAFDAC submissions, CTD dossier preparation, renewals, variations, and compliance with Nigerian regulatory frameworks. Qualified candidates should apply by sending their CV to the provided email with the job title as the subject.
- Pharmaceutical regulatory affairs role focused on NAFDAC product registration and compliance
- Requires 5+ years of regulatory affairs experience, preferably in Nigeria
- Involves CTD dossier preparation, renewals, variations, and regulatory authority liaison
- Bachelor's degree in Pharmacy, Industrial Chemistry or allied disciplines required
- Apply by emailing your CV with the job title as the subject
AI job guide
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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?
- Required5+ 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 manager, compliance, regulatoryThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in Not specifiedThe vacancy is associated with this location.
Documents to prepare
- Likely requiredUpdated CV
- Role specificCover letter or short employer message
- OptionalProfessional references
- Role specificAcademic or professional certificates
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Assistant Manager, Regulatory Affairs evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Zamiva Transnational Services and the role in Not specified.
- Add concrete examples related to manager, compliance, 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.
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Interview preparation
- What experience makes you a strong fit for this Assistant Manager, Regulatory Affairs role in manager, compliance?
- 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 Zamiva Transnational Services before the interview.
Ask what the first priorities will be in the role and how success will be measured.
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Original source description
We seeking an experienced and highly knowledgeable Regulatory Affairs Manager to lead regulatory compliance and product registration activities within our organization.
Product Registration and Dossier Management:
Prepare, review, and coordinate regulatory submissions for new pharmaceutical products.
Manage product registration, renewal, variation, and post-approval applications.
Preparation and review Common Technical Document (CTD) dossiers and supporting documents.
Ensure accuracy, completeness, and consistency of regulatory submissions.
Coordinate responses to regulatory queries and deficiency letters.
Maintain product registration status and regulatory submission trackers.
Regulatory Authority Liaison:
Act as the primary contact between the company and regulatory authorities.
Coordinate regulatory inspections, meetings, and product-related communications.
Maintain professional communication with regulatory agencies
Requirements
Bachelor's Degree in Pharmacy, Industrial Chemistry or allied disciplines.
A Master's Degree or relevant postgraduate qualification is an advantage
Minimum of Five (5) years of relevant experience in Regulatory Affairs, preferably within Nigeria.
Proven experience managing NAFDAC product registrations, renewals, variations, and regulatory submissions.
Strong knowledge of NAFDAC guidelines, SON standards, and other applicable Nigerian regulatory frameworks.
Experience in a supervisory or managerial regulatory affairs position in a pharmaceutical manufacturing environmentis preferred.
Check how your CV matches this job
Method of Application
- Interested and qualified candidates should send their detailed CV to:
- metusmetus73@gmail.com
- using the Job Title as the subject of the email
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