JOB TITLE: Regulatory Affairs Officer
JOB LOCATION: Lagos
Responsibilities
- Product registration with NAFDAC, renewals, import permits, clearing permits (for Narcotics), Laboratory analysis requests, facility inspection requests, and product dossiers review.
- Obtaining permits for orphan products with NAFDAC under service drugs provisions; global listing licenses for food and cosmetics products.
- Pharmacovigilance (safety issues about our product. Collection of product ADRs and logging into pharmacovigilance logbook that is reported to NAFDAC.
- Monthly reconciliation report for each product we market which will be returned to the affected companies and NAFDAC Pharmacovigilance centre.
- Postmarketing surveillance – any additional information besides pharmacovigilance issues that concerns our product. E.g emergence of better molecules. New indications for existing products. New formulations such as incrementally modified drugs.
- Narcotic and controlled substances distribution monitoring and reporting.
- Monitoring of cold chain and temperature-controlled logistics systems.
- Interfacing with regulatory teams of the company’s foreign trade partners under the supervision of the regulatory affairs manager.
Requirements
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- B.Pharm
- Minimum of 3 years of work experience as a regulatory officer.
- Should be familiar with agencies’ compliance processes.
Application Closing Date
Not Specified.
HOW TO APPLY
Interested and qualified candidates should send their CV to: [email protected] using the Job Title as the subject of the email.
Job Features
Job Category | Medical/ Healthcare / Pharmaceutical |