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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