Job Description
A global leader in biopharmaceuticals is seeking a Director, Global Regulatory Affairs CMC Marketed Products Development Lead in Zurich, Switzerland. You will be accountable for developing and executing GRA CMC strategies, managing regulatory submissions, and leading a team in a complex environment. The ideal candidate will have over 10 years of experience in pharmaceutical regulatory CMC and a strong background in lifecycle management. This role offers a full-time position with travel requirements of 10-30%.
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Submit ApplicationJob Details
- Location Zürich, Zürich
- Job Type Full-time
- Category Management & Operations
- Posted Date February 21, 2026
- Application Deadline April 02, 2026