Thursday, 19 July 2018

Veterinary Medicines Regulatory Affairs Consultant at Zoetis Inc

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. Zoetis serves veterinarians, livestock producers and people who raise and care for farm and companion animals with sales of its products in more than 100 countries. In 2016, the company generated annual revenue of $4.9 billion with approximately 9,000 employees.Veterinary Medicines Regulatory Affairs Consultant at Zoetis Inc

Job Title: Veterinary Medicines Regulatory Affairs Consultant

Location: Lagos

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
How to apply
Interested? Please apply by sending your resume and motivation letter

Click here to apply


Application Deadline Date
Not stated





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