Takeda Pharmaceutical Company-posted about 1 year ago
Full-time • Mid Level
Remote • Cambridge, MA
Chemical Manufacturing
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The Manager, Global Regulatory Affairs CMC Submission Management at Takeda plays a crucial role in supporting the execution of regulatory CMC tasks for investigational, registration, and post-approval activities. This position involves collaboration with cross-functional teams to develop project plans for global regulatory submissions, ensuring alignment with business objectives and timelines. The role requires managing multiple projects simultaneously and contributing to the organization's initiatives while enhancing regulatory compliance and processes.
