Regulatory Affairs Lead

3 weeks ago


Boston, Massachusetts, United States Takeda Pharmaceutical Full time
Job Overview

Takeda Pharmaceutical is seeking a highly skilled Regulatory Affairs professional to join our team as Associate Director, Global Regulatory Affairs Marketed Products.

About the Role

This role will be responsible for defining and developing global regulatory strategies to maximize regulatory success for complex and multiple projects. The successful candidate will lead the Global Regulatory Team (GRT) and applicable sub-working groups, ensuring global regulatory compliance.

Key Responsibilities:
  • Lead the GRT and represent the team at project meetings.
  • Define strategies and provide tactical guidance to teams to ensure global regulatory strategy is updated and executed.

The ideal candidate will have 8+ years of pharmaceutical industry experience, with 6 years of regulatory experience or a combination of 5+ years regulatory and/or related experience.

Requirements:
  • BSc Degree preferred, BA accepted.
Compensation:

The estimated salary range for this position is $149,100 - $234,300 per year. U.S.-based employees may be eligible for short-term and long-term incentives, medical, dental, vision insurance, a 401(k) plan, and company match.

About Us:

Takeda is transforming patient care through innovative specialty pharmaceuticals and patient support programs. We foster an inclusive, collaborative workplace where employees are united by a commitment to delivering Better Health and a Brighter Future.



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