Global Regulatory Submission Manager

Ferring Pharmaceuticals

Kastrup, Denmark
Global regulatory submissions
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.
  • The team serves as a central function in Ferring, collaborating closely with Regulatory Affairs globally and working in a fast-paced environment.

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
  • eCTD and other regulatory formats
  • electronic regulatory submissions
  • end-to-end submission lifecycle
  • document management system

Nice-to-have

  • technical flair and IT systems understanding
  • continuous improvement and cross-functional partnership
  • international, dynamic, and collaborative environment

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter