Veeva Rim Specialist, Global Regulatory Affairs

Ferring

Denmark
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Veeva rim system expertise
Regulatory gxp systems experience
End-to-end regulatory process knowledge
** Ferring Pharmaceuticals is seeking a Veeva Rim Specialist for their Global Regulatory Affairs team in Denmark. The role requires strong expertise in Veeva RIM systems and regulatory processes to enhance operational efficiency and ensure compliance within a multicultural and interdisciplinary environment. **

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 system inspection readiness while supporting faster submission processes and regulatory data transparency.
  • Ferring offers a multicultural environment where employees collaborate globally to bring science to life for patients.

Matching Summary

Match Score: 75

** Ferring Pharmaceuticals is seeking a Veeva Rim Specialist for their Global Regulatory Affairs team in Denmark. The role requires strong expertise in Veeva RIM systems and regulatory processes to enhance operational efficiency and ensure compliance within a multicultural and interdisciplinary environment. **

Skills & Requirements

Must-have

  • Veeva RIM system expertise
  • Regulatory GxP systems experience
  • End-to-end regulatory process knowledge

Nice-to-have

  • Cross-functional global collaboration
  • Analytical problem-solving skills
  • Stakeholder management capabilities

Key Requirements

  • Master's degree in Life Sciences or IT
  • Several years of Regulatory Affairs experience
  • Experience with eCTD and IDMP requirements

Work Rights

Not specified

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