2026 Summer Internship Program: Process Documentation Intern

Takeda

Lexington, MA, USA
Base: $21.00 - $46.00ph; bonus/equity: not specifi...
Onsite
Gmp documentation process
Revise sops, batch records
Technical writing experience
Responsible for GMP documentation process in support of manufacturing operations including revising SOPs, Batch Records and Form Preps

Job Summary

  • Responsible for GMP documentation process in support of manufacturing operations including revising SOPs, Batch Records and Form Preps.
  • Internship Development Opportunities include learning how to design and write documentation for a biotechnology environment, and how to effectively resource plan and manage deliverables for projects.
  • The internship program offers hands-on experience with real projects, dedicated mentorship, networking opportunities, and exposure to multiple business areas within a Pharmaceutical Organization.

Matching Summary

Responsible for GMP documentation process in support of manufacturing operations including revising SOPs, Batch Records and Form Preps.

Salary

Base: $21.00 - $46.00/hour; Bonus/Equity: Not specified; Benefits: Paid sick time, Civic Duty paid time off, Commuter Benefit

Skills & Requirements

Must-have

  • GMP documentation process
  • Revise SOPs, Batch Records
  • Technical writing experience
  • MS Office proficiency
  • Internet skills

Nice-to-have

  • Advanced document management applications
  • Continuous improvement projects
  • Strong team player
  • Attention to detail
  • Flexible

Key Requirements

  • Must be pursuing an undergraduate degree
  • Authorized to work in the U.S. without sponsorship
  • Currently enrolled in a degree program graduating December 2026 or later
  • Able to work full time 40 hours a week

Work Rights

Authorized to work in the U.S. without sponsorship

Tailored Resume

Cover Letter