Global Regulatory Affairs Lead: Strategy & Submissions
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Pharmaceutical
Regulatory Compliance Specialist -
Management
Regulatory Compliance Specialist
Job Description & How to Apply Below
Takeda in Cambridge, MA seeks an Associate Director to define and lead global regulatory strategies for complex programs, providing strategic and tactical guidance to cross-functional teams while ensuring compliance with FDA and global regulatory requirements.
The role oversees US FDA submissions, stakeholder communications, and staff mentorship in a hybrid work setting. A scientific advanced degree and 6+ years in pharma with regulatory experience are preferred.
We have an opening for a Global Regulatory Affairs Lead:
Strategy & Submissions in Cambridge, MA, United States within Legal, Management & Operations.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Global Regulatory Affairs Lead:
Strategy & Submissions role in the description above.
We appreciate your interest in this position.
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