Veeva Rim Specialist, Global Regulatory Affairs

FERRING PHARMACEUTICALS AS

Denmark
Not specified (assumed hybrid based on collaborative nature).
Veeva vault rim experience
Regulatory gxp systems knowledge
End-to-end regulatory process support
Ferring Pharmaceuticals is seeking a Veeva Rim Specialist with expertise in regulatory GxP systems to enhance business operations within Global Regulatory Affairs. The ideal candidate will bridge the gap between various teams, ensuring optimal use of Veeva systems for regulatory document and submission management

Job Summary

  • The role serves as the key interface between Regulatory Affairs, IT, and external vendors to translate business needs into system enhancements.
  • Candidates will ensure inspection readiness and lead impact assessments for Veeva RIM releases in a global environment.
  • Ferring Pharmaceuticals offers an empowering culture focused on scientific advances in reproductive health, gastroenterology, and urology.

Matching Summary

Match Score: 85

Ferring Pharmaceuticals is seeking a Veeva Rim Specialist with expertise in regulatory GxP systems to enhance business operations within Global Regulatory Affairs. The ideal candidate will bridge the gap between various teams, ensuring optimal use of Veeva systems for regulatory document and submission management.

Skills & Requirements

Must-have

  • Veeva Vault RIM experience
  • Regulatory GxP systems knowledge
  • End-to-end regulatory process support
  • System change request implementation
  • Stakeholder management across IT and Quality

Nice-to-have

  • Global cross-functional collaboration
  • Analytical problem-solving skills
  • Structured project management approach
  • Experience with eCTD and IDMP requirements

Key Requirements

  • Master's degree in Life Sciences or IT
  • Several years of Regulatory Affairs experience
  • Hands-on ownership of Veeva RIM applications

Work Rights

Not specified

Tailored Resume

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