Regulatory Affairs Manager

vor 1 Woche

Zürich, Zürich, Schweiz Pfizer Vollzeit
Regulatory Affairs Manager (M/F/d)

time type: 60%/80%/100%

This is what you can look forward to:

  • Overseeing assigned product portfolio of innovative prescription drugs with complex regulatory background
  • Handling entire regulatory lifecycle from initial MAAs to line extensions, labeling and CMC variations, renewals, PSUR submissions, etc.
  • Developing of submission strategies to enhance the product value and expedite pathways
  • Collaborating with local and global regulatory and crossfunctional colleagues
  • Acting as reliable and competent contact for Swissmedic

What you offer:

  • Academic degree in natural sciences
  • At least 3 year experience in Swiss Regulatory Affairs
  • Extensive knowledge of the current Swiss regulatory and drug laws environment, knowledge about other legal environments (EU, US, etc.) is of advantage
  • Very good knowledge of German and English, good knowledge of French and/or Italian is of advantage
  • Solid knowledge of pharmaceutical analytics technology, pharmacology, toxicology and medicine
  • Good computer skills
  • Knowledge of or experience in project management techniques is of advantage
  • Strong skills in productivity, organizational and time management
  • Highest quality standards
  • Demonstrated ability to foster teamwork

What we offer:

  • An attractive overall employment package (compensation, vacation, pension) in a worldleading company
  • An exciting, fastpaced environment
  • Friendly, open and collaborative company culture
  • Being part of a local as well as an interdisciplinary team
  • Flexible working hours
  • Opportunities to engage in social projects
  • Companypaid health activity program
  • Great growth
- and development opportunities

  • Health programs for all employees
  • The opportunity to engage in social projects
Convinced?

LI-PFE

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