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⏰ Full-time

Manager, Regulatory Affairs

Takeda Pharmaceuticals
Location 📍 Gurgaon, India
Posted 📅 June 04, 2026
Work Type ⏰ Full-time

Position Overview

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice (https://jobs.takeda.com/privacynotice) and Terms of Use (https://www.takeda.com/terms-and-conditions/) . I further attest that all information I submit in my employment application is true to the best of my knowledge.

**Job Description**

**OBJECTIVES/PURPOSE** :

Manager Regulatory Affairs ensures obtaining regulatory approval for products and life cycle management of products and regulatory submission with Indian Health Authority (CDSCO) and NMRA Sri Lanka. This role helps Takeda navigate complex regulatory landscapes, ensuring regulatory compliances with respect to the Health Authority and facilitating the successful maintenance of products registration and licenses.

**KEY JOBS ACCOUNTABILITIES** :

+ Managing regulatory app...

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Job Details

Employment Type
Full-time
📊
Category
other-general
🏠
Work Arrangement
On-site
📍
Location
Gurgaon, India