Global Regulatory Submission Manager

Ferring Pharmaceuticals

Kastrup, Denmark
Global regulatory submissions experience
Ectd and other regulatory formats
Electronic regulatory submissions
You will play an active role throughout the entire submission lifecycle—from planning regulatory activities to final publishing

Job Summary

  • You will play an active role throughout the entire submission lifecycle—from planning regulatory activities to final publishing.
  • You will join a small, dedicated Global Submission Management team of experienced colleagues, responsible for electronic regulatory submissions across multiple regions.
  • To succeed in this position, you need technical flair and IT systems understanding, as well as the ability to bring structure and clarity to everything you do.

Matching Summary

You will play an active role throughout the entire submission lifecycle—from planning regulatory activities to final publishing.

Skills & Requirements

Must-have

  • Global Regulatory Submissions experience
  • eCTD and other regulatory formats
  • electronic regulatory submissions
  • cross-functional teams collaboration
  • prioritizing multiple projects

Nice-to-have

  • technical flair and IT systems understanding
  • continuous improvement mindset
  • international, dynamic, and collaborative environment

Key Requirements

  • Hands-on experience with publishing system
  • Knowledge of eCTD requirements
  • Proven experience in Regulatory Affairs
  • Relevant master’s degree or work experience
  • Candidates must be located in the Øresund region

Work Rights

Not specified

Tailored Resume

Cover Letter