Regulatory Affairs Director

4 days ago


Copenhagen, Copenhagen, Denmark Genmab AS Full time

We are seeking a skilled and experienced Regulatory Affairs Director to join our team at Genmab A/S. As a key member of our Regulatory Affairs CMC team, you will be responsible for providing strategic regulatory guidance and support for the development and commercialization of our biologic products.

The ideal candidate will have a strong understanding of global regulatory requirements and experience in developing and executing sound and robust regulatory strategies for biological products during early and late stage development, and lifecycle.

Key Responsibilities:
  • Develop and execute sound and robust global regulatory CMC strategies for biological products during early and late stage development, and lifecycle.
  • Collaborate with cross-functional peers to facilitate and optimize product development.
  • Plan, review, and prepare CMC documentation for clinical applications, marketing authorization applications, and health authority briefing packages.
  • In collaboration with CMC, plan and prepare responses to health authority information requests.
  • Provide advice and guidance on EU, US, and selected worldwide regulatory legislation for CMC topics.

About You:

  • You have excellent collaboration and communication skills.
  • You thrive being challenged and working in cross-functional teams.
  • You are able to work independently with an ability to drive projects to successful outcomes.
  • You have a quality mindset and are able to prioritize your work in a fast-paced and changing environment.
  • You are result-oriented and committed to contributing to the overall success of Genmab.


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