Nordic Regulatory Affairs Manager (Nordics - 121)

Nordic Regulatory Affairs Manager (Nordics - 121)

Zoetis Animal Health

Copenhagen, Denmark

A glimpse of your new workday with us

In this position, you will be responsible for many diverse tasks within RA, QA, and PV. From managing RA changes to our many products to handling QA issues of varying complexity, in close collaboration with our internal supply and manufacturing function and external distribution partners, to reporting and filing adverse reaction cases. You will be responsible for our local Quality Management System (QMS), ensuring its ongoing suitability for our business needs.

Core responsibilities

Your work will consist of various tasks within the areas of:

  • License renewals, variations, and new applications incl artwork.
  • Quality.
  • Regulatory strategy.
  • Maintenance of regulatory databases.
  • Compliance and Pharmacovigilance.
  • Industry and corporate affairs relations.

You will be a manager in a small Nordic team, ensuring excellent support to our commercial and supply teams, close contact, and direction - even at a distance.

In this role, it is vital that you develop constructive cross-functional relationships with colleagues across the region and the Zoetis business. By contributing to our local RA/QA/PV departmen structure and through direct contact with the Nordic authorities, you actively drive the regulatory direction.

Analytical, communicating, and effective

  • To have success in this position, you must have an analytical mind with strong attention to detail and problem-solving skills as well as good communication skills, written and verbal.
  • You hold a commercial understanding and can unfold effective time management and prioritization in a workday with sometimes multiple and overlapping deadlines.
  • You are fluent in Danish and English and have a knowledge of one or more regional local languages.

Your education and experience

  • A degree in pharmacy, veterinary sciences, or related fields and/or a minimum of 3-5 years of experience within Regulatory Affairs.
  • Authority and experience to be a Responsible Person in DK.
  • Experience or knowledge of the animal health industry.
  • Understanding of regulatory environment and trends, including legislative, market, and industry competitor developments.
  • Detailed knowledge of relevant European legislation, licensing, and related practices and laws.
  • IT literate. Able to use standard business software, communication tools, and quality management systems.
  • Excellent Danish and English skills (written and verbal).

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© EuroJobsites 2021

EuroJobsites is a registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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