Regulatory Affairs Manager

Vor 5 Tagen

Zürich, Zürich, Schweiz Hays Vollzeit


Location:
Zurich |
Contract:
March–August 2026

Are you passionate about shaping the future of vaccines? Join the Regulatory Affairs Vaccines team of our globally renowned client and play a key role in driving regulatory strategies across Europe.

What you'll do:

  • Lead regulatory activities for vaccine projects, including submissions and lifecycle management.
  • Prepare and manage Marketing Authorization Applications (MAA) and variations in compliance with EMA and local regulations.
  • Ensure timely and accurate regulatory documentation and filings.
  • Provide oversight for assigned clinical trials and related regulatory requirements.
  • Collaborate with global and regional teams to align regulatory strategies.
  • Support health authority interactions and meetings in the region.
  • Maintain regulatory archives and manage documentation in EDMS.
  • Track regulatory commitments and activities in internal systems.

What we're looking for:

  • Bachelor's degree; minimum 6 years in pharma, including 3+ in regulatory affairs.
  • Proven experience with vaccines/biologics and EMA submissions.
  • Strong understanding of regulatory strategy and scientific issues.
  • Excellent communication, organizational, and negotiation skills.
  • Ability to manage multiple projects and meet timelines.
  • Team player with proactive problem-solving skills.
  • High attention to detail and quality focus.
  • Willingness to travel (~10%).


Ready to make an impact? Apply now and help us deliver innovative vaccines to patients worldwide

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