Head Of Parenteral Drug Products (vice President)

Takeda UK

Boston, MA, US
Base: $259,000.00 - $407,000.00; bonus/equity: sho...
Hybrid
Parenteral drug product strategy
Aseptic fill/finish process development
Lyophilization cycle design and scale-up
This role leads the global Parenteral Drug Product organization, setting strategy for robust formulations and aseptic fill/finish processes from early phase through commercialization

Job Summary

  • This role leads the global Parenteral Drug Product organization, setting strategy for robust formulations and aseptic fill/finish processes from early phase through commercialization.
  • The successful candidate will own parenteral CMC deliverables for global submissions including IND, BLA, and NDA filings while driving lifecycle management for commercial products.
  • Takeda offers a competitive base salary range of $259,000.00 - $407,000.00 along with comprehensive benefits including medical insurance, 401(k) matching, and up to 120 hours of paid vacation.

Matching Summary

This role leads the global Parenteral Drug Product organization, setting strategy for robust formulations and aseptic fill/finish processes from early phase through commercialization.

Salary

Base: $259,000.00 - $407,000.00; Bonus/Equity: Short-term and/or long-term incentives eligible; Benefits: Medical, dental, vision, 401(k) match, disability, life insurance, tuition reimbursement, 80 hours sick time, 120 hours vacation

Skills & Requirements

Must-have

  • Parenteral drug product strategy
  • Aseptic fill/finish process development
  • Lyophilization cycle design and scale-up
  • Container closure system expertise
  • Global CMC regulatory submissions
  • Tech transfer to CMOs and sites

Nice-to-have

  • Executive leadership presence
  • Diversity and inclusion mindset
  • Innovative problem solving skills
  • Cross-functional team collaboration
  • Strategic negotiation abilities

Key Requirements

  • PhD in related field with 15+ years experience
  • Masters degree with 20+ years experience
  • Bachelors degree with 25+ years experience
  • Proven track record in global parenteral CMC regulatory strategy
  • Experience leading tech transfer and PPQ execution

Work Rights

Not specified

Tailored Resume

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