Viimsi, Estonia

Msc / Bsc


Regulatory Affairs Officer

Step into the world of Interchemie as a Specialist in Regulatory Affairs. Work closely with various stakeholders such as your colleagues, clients, agents, and authorities. As a regulatory expert, you ensure our extensive range of over 100 veterinary medicines, produced under GMP standards, meets the requirements of regulatory bodies around the world. This challenging role offers you the opportunity to manage projects from start to finish and work with satisfaction on your personal and professional development. At Interchemie, you are the conductor of your success!

Your Job

As a Regulatory Affairs Specialist at Interchemie, you are responsible not just for one aspect but collaborate with your colleagues from A to Z in registering a wide range of existing and new veterinary medicines. Your main goal is to ensure that registration dossiers for the relevant products are submitted in the relevant countries. This is no small feat, as we sell our products in over 120 countries and are an order-driven organisation. Therefore, you work closely with our sales department to align production planning with their plans and activities in global markets.

In this crucial role, “ownership” is a key term. You are expected to display independence and professionalism in carrying out your duties. If you are at the start of your career, do not worry, as we offer challenging roles and guidance for your personal and professional growth. We take pride in being able to train and educate new RA colleagues.

Your responsibilities include:

  • Preparing registration dossiers, including analytical, chemical, toxicological, residue, and clinical studies.
  • Responsible for compiling and reviewing product-specific documentation and registering new and existing veterinary medicines.
  • Acting as a liaison for internal and external stakeholders and RA teams.
  • Providing regulatory input for appropriate follow-up of inspections and audits.
  • Staying informed about developments and trends in Regulatory Affairs and Registration to deliver the best results for Interchemie and its clients.

Employer Features

About Interchemie

From its humble beginnings in The Netherlands, Interchemie is now supplying partners worldwide with veterinary products including veterinary medicines, nutritional products and disinfectants. We offer our products to careful selected distributors worldwide in Europe, Asia, Africa, South America and the Middle-East. Interchemie produces according to GMP and GMP+ guidelines.

Interchemie operates three production facilities. With 12 production lines, namely: injectables lines, oral liquids lines and water-soluble powders lines. Interchemie has attained this high quality standard by continuously researching and developing new products. Because only by improving our product line can we safeguard the health of animals in the future.

In Estonia you’ll find about 150 motivated colleagues in our production facility and our neighbouring packaging facility. We are located on the beautiful peninsula of Viimsi in the North of Tallinn near the Gulf of Finland (Soome lath). Our organisation is evolving and growing. A recent change of management sees us working in a more open, cooperative way with greater ownership and focus on (human) potential. Our CEO tries to visit each department every month to discuss challenges and goals (of the company) and actively wishes input from the departments – involvement, ownership and expertise are keywords.

Uku Rooni

Regulatory Affairs Specialist

"Don’t be shy to contact! Give opportunities a chance to evolve into something more."

People and products you can rely on

The Faces Behind Our Success

Your Colleagues


  • Interesting challenges and a family-like company culture
  • Highly skilled team and high quality resources
  • Sharpen your skills and deepen your expertise
  • Growing and evolving organisation
  • Bonus on top of salary


  • A master’s degree in a relevant field (e.g., Biology, Chemistry, Biotechnology, or other Life Sciences)
  • Relevant work experience in Regulatory Affairs
  • Project management skills, initiative, and flexibility
  • Good skills in Business English

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