Global Manufacturing Sciences Process Science Lead – Small Molecules Api (sr. Manager)

Takeaweigh

Boston, MA, USA
Base: $137,000.00 - $215,270.00; bonus/equity: not...
Small molecule api manufacturing
Process design and scale-up
Technology transfer
This senior individual contributor role is the subject matter expert and primary technical contact for Takeda’s small molecule API manufacturing for synthetic drug substance across the product lifecycle

Job Summary

  • This senior individual contributor role is the subject matter expert and primary technical contact for Takeda’s small molecule API manufacturing for synthetic drug substance across the product lifecycle.
  • You will define and drive phase-appropriate, fit-for-purpose manufacturing strategies, applying deep drug substance expertise and direct manufacturing experience to support process design, scale-up, technology transfer, and commercial supply.
  • U.S. Base Salary Range: $137,000.00 - $215,270.00; Bonus/Equity: Not specified; Benefits: Medical, dental, vision, 401(k), disability, life insurance, tuition reimbursement, paid volunteer time off, holidays, well-being benefits.

Matching Summary

This senior individual contributor role is the subject matter expert and primary technical contact for Takeda’s small molecule API manufacturing for synthetic drug substance across the product lifecycle.

Salary

Base: $137,000.00 - $215,270.00; Bonus/Equity: Not specified; Benefits: Medical, dental, vision, 401(k), disability, life insurance, tuition reimbursement, paid volunteer time off, holidays, well-being benefits

Skills & Requirements

Must-have

  • Small molecule API manufacturing
  • Process design and scale-up
  • Technology transfer
  • Commercial supply support
  • Troubleshoot manufacturing issues
  • CMC regulatory submissions

Nice-to-have

  • Antibody-Drug Conjugates (ADCs) expertise
  • Continuous improvement
  • Inspection readiness culture
  • Sustainability improvements

Key Requirements

  • MSc or PhD in Chemistry, Chemical Engineering, Pharmacy
  • At least 5 years pharmaceutical industry experience
  • Direct pilot plant manufacturing experience
  • Strong understanding of ICH and global regulatory guidelines
  • Experience with phase-appropriate development
  • Demonstrated experience authoring CMC sections
  • Proven SME-level experience within quality systems

Work Rights

Not specified

Tailored Resume

Cover Letter