Head Of Oral Drug Products (vice President)

Takeda

Boston, MA, US
Base: $259,000.00 - $407,000.00; bonus/equity: eli...
Hybrid
Global oral drug product strategy leadership
Oral solid dose formulation expertise
Process development and scale-up experience
This role leads the global Oral Drug Product organization and delivery of oral drug product development from early phase through commercialization and lifecycle management

Job Summary

  • This role leads the global Oral Drug Product organization and delivery of oral drug product development from early phase through commercialization and lifecycle management.
  • The position is accountable for oral drug product design and development including selection of dosage form, excipients, and process pathway consistent with target product profile.
  • U.S. based employees are eligible for short-term and long-term incentives along with comprehensive benefits including medical, dental, vision, and a 401(k) plan match.

Matching Summary

This role leads the global Oral Drug Product organization and delivery of oral drug product development from early phase through commercialization and lifecycle management.

Salary

Base: $259,000.00 - $407,000.00; Bonus/Equity: Eligible for short-term and/or long-term incentives; Benefits: Medical, dental, vision, 401(k) match, disability, life insurance, tuition reimbursement, paid time off

Skills & Requirements

Must-have

  • Global oral drug product strategy leadership
  • Oral solid dose formulation expertise
  • Process development and scale-up experience
  • CMC regulatory submission management
  • Tech transfer to CMOs and internal sites
  • QbD principles and control strategy design

Nice-to-have

  • Continuous manufacturing knowledge
  • 3D printing and hot-melt extrusion skills
  • Pediatric and geriatric formulation strategies
  • Innovation mindset and change leadership
  • Cross-functional stakeholder partnership skills

Key Requirements

  • 25+ years relevant industry experience with Bachelor's degree
  • 20+ years relevant industry experience with Master's degree
  • 15+ years relevant industry experience with PhD
  • Demonstrated people and program management skills
  • Expertise in writing regulatory documents

Work Rights

Not specified

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