Regulatory Associate

☞ Krka

View: 130

Update day: 26-11-2025

Location: Sint-Niklaas East Flanders

Category: Other

Industry: Pharmaceuticals

Position: Entry level

Job type: Full-time

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Job content

Excellence is part of us! Krka is one of the leading generic pharmaceutical companies worldwide. We appreciate the knowledge and promote creativeness. We provide optimum working conditions. Creativity is our way of life and excellence is part of us.

KRKA Belgium would like to invite to our team

REGULATORY ASSOCIATE

Search parameters:

  • Education: University degree in preferably pharmaceutical Sciences (B. Sc./M. Sc.).
  • Experience: Junior level
  • Languages: Proficiency in Dutch and English. Very good understanding of written French and written German.
  • The ability to produce high-quality product information (PI) texts.
  • Strong linguistic skills and the ability to translate between English, French, German or Dutch.
  • Ability to work effectively in a highly regulated field.
  • Ability to put attention to detail also in routine work.
  • The candidate should be able to prioritize and work effectively also under time pressure.
  • Excellent PC use skills with regard to Word-processing, spreadsheets, database applications, and the internet. The work includes text editing.

    • After initial training the major working assignments would be:

  • Your main task will be producing, maintaining, and editing PI texts.
  • Supporting regulatory processes on the local level in close cooperation with Deputy Director for area Regulatory Affairs. This includes the preparation of translations and ensuring their timely submission, regularly interacting with local authorities and Krka colleagues regarding product-related activities, and providing supplemental information for ongoing procedures.
  • Verification and approval of artworks according to the last approved PI.
  • Ensuring compliance with local regulatory requirements and Krka’s policies and standard operating procedures in the fields of Regulatory Affairs, Good Distribution Practice, Pharmacovigilance, and Publicity and Information.
  • Adequately supporting other functions to enable compliance in areas related to regulatory affairs.
  • Be constantly updated on relevant EU and local regulations and guidelines.
  • Handling customer complaints and other quality tasks.
  • Maintaining a positive relationship with internal and external regulatory contacts and other stakeholders.

    • Please send your CV with a motivational letter attached via LinkedIn. We are looking forward to your applications.

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    Deadline: 10-01-2026

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