Strategic Regulatory Affairs Director

Vor 5 Tagen


Zug, Zug, Schweiz TN Switzerland Vollzeit
Job Overview

We are seeking a highly skilled Associate Director to lead our Global Regulatory Affairs team in Zug, Switzerland. As part of our TN Switzerland organization, you will be responsible for developing and executing regulatory strategies for precision medicine and digital health assets.

This role requires a strong understanding of global regulatory requirements, as well as the ability to work effectively with cross-functional teams within GSK.

  • Key Responsibilities:
  • Develop and execute global regulatory strategies for precision medicine and digital health assets.
  • Lead interactions with local and regional regulatory authorities.
  • Ensure compliance with internal processes and policies, as well as regional regulatory requirements.
  • Collaborate with experimental medicine and digital health teams to drive business objectives.
Requirements

To succeed in this role, you will need:

  • Bachelor's degree in biological science, healthcare science, or engineering.
  • Experience in regulating companion diagnostics and SaMD within a pharmaceutical company.
  • Proven track record of leading global development, submission, and approval activities.
  • Strong communication and facilitation skills.
  • Ability to build and maintain relationships with stakeholders.


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