Regulatory Affairs Associate for managing new drug registrations and preparing documentation in the India Market. Collaborating with stakeholders and supporting compliance in bulk drug registration.
About the role
- Internship in Global Regulatory Affairs at Takeda, supporting development and regulatory submissions. Gain hands-on experience in a leading pharmaceutical R&D organization.
Responsibilities
- Learn about various Regulatory CMC functions involved in the development of new products through the maintenance of marketed products post health authority approval.
- Gain valuable experience of the complexities of regulatory requirements.
- Interact with leaders involved in the development and execution of strategic plans through product life cycle.
Requirements
- Must be pursuing a Masters, and/or Doctoral Degree in Chemistry, Pharmaceutical Sciences, Regulatory Affairs, Biochemistry, Life Sciences, or related fields.
- Must be authorized to work in the U.S. on a permanent basis without requiring sponsorship
- Must be currently enrolled in a degree program graduating December 2026 or later
- The intern must be able to commit to one of these time frames
- Able to work full time 40 hours a week during internship dates
Benefits
- Paid sick time
- Civic Duty paid time off
- Participation at company volunteer events
- Participation at company sponsored special events
- Access to on-site fitness center (where available)
- Commuter Benefit: To offset your work-commute expenses, Takeda provides U.S. employees with a fixed monthly subsidy to be used for either public transportation (transit) or parking.
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