Director, Pharmaceutical Sciences Program Leadership

Takeda UK

Boston, MA, USA
Base: $177,000.00 - $278,080.00; bonus/equity: not...
Pharmaceutical development acumen
Scientific leadership and innovation
Global cmc development teams
Provides strategic scientific leadership and program management for multiple global CMC development teams dealing with complex development programs that require scientific depth and overall product development acumen for successful execution

Job Summary

  • Provides strategic scientific leadership and program management for multiple global CMC development teams dealing with complex development programs that require scientific depth and overall product development acumen for successful execution.
  • Mentors other members of the department to develop their abilities to lead and advance their individual skills of pharmaceutical product development.
  • Develops and communicates convincing business cases for department strategies that motivate stakeholders to take action.

Matching Summary

Provides strategic scientific leadership and program management for multiple global CMC development teams dealing with complex development programs that require scientific depth and overall product development acumen for successful execution.

Salary

Base: $177,000.00 - $278,080.00; Bonus/Equity: Not specified; Benefits: Medical, dental, vision, 401(k), disability, life insurance, tuition reimbursement, paid volunteer time off, holidays, well-being benefits, sick time, vacation

Skills & Requirements

Must-have

  • pharmaceutical development acumen
  • scientific leadership and innovation
  • global CMC development teams
  • risk identification and mitigation
  • cross-divisional initiatives
  • pharmaceutical product development

Nice-to-have

  • inspire commitment and influence
  • mobilize high performance
  • anticipate future needs
  • develop capabilities
  • champion change and role model
  • humility and approachability

Key Requirements

  • BS + 18 years; MS + 16 years; PhD + 10 years
  • Expert knowledge of pharmaceutical development
  • Extensive knowledge of cGMP, ICH Guidelines
  • Experience in global regulatory submission requirements

Work Rights

Not specified

Tailored Resume

Cover Letter