Senior Gxp System And Process Specialist, Global Regulatory Affairs

Ferring Pharmaceuticals

Denmark
Not specified (assumed to be hybrid or onsite based on company culture)
Veeva rim applications
Regulatory gxp systems
Regulatory document management
Ferring Pharmaceuticals is seeking a Senior GxP System and Process Specialist with expertise in Veeva RIM and regulatory GxP systems to enhance their regulatory processes. The ideal candidate will possess a strong background in Regulatory Affairs, relevant technical skills, and the ability to work in a multicultural environment

Job Summary

  • Drive business system operations and ensure optimal use of Veeva RIM systems in Ferring, supporting regulatory document management, submission management and information management.
  • Act as the key interface between Regulatory Affairs, IT and external vendors, translating business needs into system enhancements.
  • You will be working in a multicultural and interdisciplinary environment with colleagues and user community located throughout the global Ferring organisation.

Matching Summary

Match Score: 85

Ferring Pharmaceuticals is seeking a Senior GxP System and Process Specialist with expertise in Veeva RIM and regulatory GxP systems to enhance their regulatory processes. The ideal candidate will possess a strong background in Regulatory Affairs, relevant technical skills, and the ability to work in a multicultural environment.

Skills & Requirements

Must-have

  • Veeva RIM applications
  • Regulatory GxP systems
  • Regulatory document management
  • Submission management
  • Information management
  • System inspection readiness

Nice-to-have

  • Analytical and problem-solving skills
  • Structured and proactive approach
  • Stakeholder management skills
  • Cross-functional collaboration

Key Requirements

  • Master’s degree in Life Sciences or IT/Science
  • Several years of experience in Regulatory Affairs or Regulatory Operations
  • Hands-on experience with Veeva Vault RIM
  • Experience with system ownership/product ownership/application management
  • Understanding of regulatory end-to-end processes
  • Familiarity with global regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter