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Veterinary Medicines Regulatory Affairs consultant

Veterinary Medicines Regulatory Affairs consultant (BE-ZAV/GVD-279) Nigeria

You are:

  • Looking for a challenging job in an international environment.
  • Strong in building good relationships with various stakeholders.
  • Able to multi-task and work to stringent timelines
  • Outstanding in quality maintenance
  • A problem-solver, able to think outside the box.
  • Willing to travel, up to 5%

You have:

  • Excellent communication, negotiation and interpersonal skills, ensuring the ability to interact effectively with external regulators/agencies in a professional manner.
  • Proven leadership, network building and team player skills.
  • Strong oral and written English language skills.
  • BSc in Veterinary Medicines or related fields
  • Consultant accredited by NAFDAC
  • At least 7 Years direct NAFDAC experience
  • Excellent knowledge of local legal environment and requirements
  • Effective organizational skills

Your key responsibilities:

  • To 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-operation
  • Responsible for supporting Regulatory Affairs domestically
  • Submission of new product registrations including adaption of global dossier to local format
  • Participate in workshops and meetings organized by NAFDAC
  • Ensure that our company's products comply with the regulations of Nigeria
  • Keep up to date with national and international legislation, guidelines and customer practices
  • Collect, collate and evaluate scientific data from a range of sources
  • Develop and write clear arguments and explanations for new product licences and licence renewals
  • Monitor and set timelines for licence variations and renewal approvals
  • Work with specialist computer software and resources
  • Advise stakeholders and manufacturers on regulatory requirements
  • Provide strategic advice to senior management throughout the registration of a new product
  • Undertake and manage regulatory inspections
  • Liaise with, and make presentations to, regulatory authorities
  • Negotiate with regulatory authorities for marketing authorisation
  • Specify storage, labelling and packaging requirements.

Our offer:

  • An innovative, international working environment.
  • A position in a world-leading, talented and passionate Regulatory team in the number 1 Global Animal Health Company.
  • Exposure to a broad portfolio of Animal Health product portfolio.
  • Ability to build a strong international network within the Industry

Interested? Please apply by sending your resume and motivation letter

We look forward to your application.

 

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