Обзор
• The role requires accurate and up‑to‑date maintenance of all regulatory with regulatory-relevant data up to 95% compliance e.g. DRAGON and proper archiving of related records.
• Ensures that compliance activities are executed in an accurate and timely manner including but not limited to submission of safety labelling changes, safety communications, audit preparation, performance management, tracking of quality assessments, timely communication and resolution of compliance-related issues.
• Implementation of Regulatory Affairs processes and quality standards according to governing SOPs and policies, regularly track and provide updates on changes to regulatory guidance.
• Support the RA Team in labelling management including tracking and submission of labelling changes and related activities for all Novartis products.
• Maintaining open communication with internal stakeholders including Regulatory Affairs Teams, Supply Chain, CMC, Labelling, NTO and others as required and regularly provide feedback.
• Develop and maintain good working relationships with the Health Authority.
About the Role
Major Accountabilities
Regulatory Submissions & Product Lifecycle Management
· Prepare local dossiers and submit drug registration applications in a timely manner, maintain regular communication with HA during evaluation phase to support favourable approval outcomes.
· Support lifecycle maintenance activities, including renewals and post‑approval changes, ensuring on-time submissions.
· Maintain regulatory databases with accurate and up-to-date product information.
Health Authority Engagement
· Liaise with the Health Authority on submitted applications, provide timely feedback and follow-up for approvals.
· Build and maintain strong working relationships with Health Authority officials.
Compliance & Quality Activities
· Ensure compliance to global and local KPIs
· Ensure timely handling of non-compliance issues and urgently escalate compliance issues through appropriate channels and provide necessary support for resolution.
· Support audit readiness and compliance assessments.
· Contribute to data consistency and quality control reviews including comparative assessments of relevant SOP’s and other processed/documents as required.
Document and Database Management
· Maintain accurate technical and non-technical documentation change system.
· Maintain DRAGON and other relevant databases with up to date and accurate product
· information under the supervision of the RA Managers.
· Support data consistency management and CCEx activities.
Labelling Management
· Support submission and tracking of labelling updates.
· Contribute to labelling improvement initiatives and regulatory guideline reviews.
· Support maintenance country‑specific regulatory presentations for products registered in Anglophone West Africa.
· Timely escalation of issues related to product labelling and support in resolution.
Regulatory Intelligence
- Conduct consistent periodic regulatory guideline/policy reviews and communicate outcome of the reviews including the impact of identified changes.
- Communicate and emerging regulatory changes in a timely manner such as changes to Health Authority processes
Stakeholder Engagement & Internal Collaboration
· Maintain open communication with internal stakeholders including Supply Chain, CMC, Labelling, NTO, other RA teams and other relevant parties.
· Ensure distributors receive necessary documentation to support compliant importation.
Other Responsibilities
· Provide support to assigned Regulatory Affairs projects and tasks and complete delegated tasks.
· Appropriate communication of identified issues related to compliance and regulatory
intelligence affecting lifecycle management and any other issues deemed relevant.
Key Performance Indicators
• Timely registration of new drug products and re-registration of approved products
• Timely submission of post-approval changes (variations) and follow up with the Health Authority for approval.
• Ensure compliance with relevant Health authority guidelines and regulations
• Address issues related to compliance with urgency as appropriate
• Accurate monitoring and maintenance of relevant regulatory information management system(e.g. DRAGON, NRV, Production Transfer Tool)
• Achieve 95% Regulatory compliance deliverables (compliance with relevant databases, trainings and any such deliverable)
•
Education: B. Pharm
Languages: Fluent in English (mandatory)
Experiences: Minimum 1-2 years RA experience
Good understanding of CTD dossier format
Good understanding of the regulatory landscape in Nigeria/Anglophone West Africa
Detail-oriented and organized
Good communication, negotiation and inter-personal skills.
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