Veterinary Medicines Regulatory Affairs Consultant at Zoetis

Zoetis is the leading animal health company, dedicated to supporting its customers and their businesses. Building on more than 60 years of experience in animal health, Zoetis discovers, develops, manufactures and markets veterinary vaccines and medicines, complemented by diagnostic products, genetic tests, biodevices and a range of services.We are recruiting to fill the position below:Job Title: Veterinary Medicines Regulatory Affairs Consultant Ref: BE-ZAV/GVD-279Location: NigeriaYou AreLooking for a challenging job in an international environment.Strong in building good relationships with various stakeholders.Able to multi-task and work to stringent timelinesOutstanding in quality maintenanceA problem-solver, able to think outside the box.Willing to travel, up to 5%Your Key ResponsibilitiesTo support and facilitate the regulatory approval and maintenance of new and exciting veterinary products, as well as maintain in-line veterinary products in Nigeria.The Regulatory Affairs Consultant will develop relationships with representatives of NAFDAC to ensure effective communication and co-operationResponsible for supporting Regulatory Affairs domesticallySubmission of new product registrations including adaption of global dossier to local formatParticipate in workshops and meetings organized by NAFDACEnsure that our company's products comply with the regulations of NigeriaKeep up to date with national and international legislation, guidelines and customer practicesCollect, collate and evaluate scientific data from a range of sourcesDevelop and write clear arguments and explanations for new product licences and licence renewalsMonitor and set timelines for licence variations and renewal approvalsWork with specialist computer software and resourcesAdvise stakeholders and manufacturers on regulatory requirementsProvide strategic advice to senior management throughout the registration of a new productUndertake and manage regulatory inspectionsLiaise with, and make presentations to, regulatory authoritiesNegotiate with regulatory authorities for marketing authorisationSpecify storage, labelling and packaging requirements. 

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