Associate Director, Gra Business Process Office

Takeda

Massachusetts, US
Base: $153,600.00 - $241,340.00; bonus/equity: not...
Hybrid
Global regulatory affairs
Business process office
Process optimization
The Associate Director, Global Regulatory Affairs (GRA) Business Process Office (BPO) is a key contributor and business partner who supports continuous improvement, process optimization, and operational maturity efforts across the GRA organization

Job Summary

  • The Associate Director, Global Regulatory Affairs (GRA) Business Process Office (BPO) is a key contributor and business partner who supports continuous improvement, process optimization, and operational maturity efforts across the GRA organization.
  • By leading continuous improvement initiatives, applying Lean / Six Sigma and change management methodologies, and driving sustainable cross-functional adoption of improved ways of working, they contribute to advancing GRA’s operational effectiveness, compliance with Regulatory requirements and internal company standards, and alignment with strategic business goals.
  • This position is currently classified as "remote" following Takeda's Hybrid and Remote Work policy.

Matching Summary

The Associate Director, Global Regulatory Affairs (GRA) Business Process Office (BPO) is a key contributor and business partner who supports continuous improvement, process optimization, and operational maturity efforts across the GRA organization.

Salary

Base: $153,600.00 - $241,340.00; Bonus/Equity: Not specified; Benefits: Medical, dental, vision insurance, 401(k) plan and company match, disability coverage, life insurance, tuition reimbursement, paid volunteer time off, company holidays, well-being benefits, sick time, paid vacation

Skills & Requirements

Must-have

  • Global Regulatory Affairs
  • Business Process Office
  • process optimization
  • Lean / Six Sigma methodologies
  • change management methodologies
  • cross-functional adoption

Nice-to-have

  • patient-focused company
  • foster an inclusive, collaborative workplace
  • advancing GRA’s operational effectiveness
  • alignment with strategic business goals

Key Requirements

  • Bachelor’s degree in Life Sciences, Business Administration, or related field
  • 7+ years of experience in pharmaceutical and/or biotech industry
  • 4+ years of experience in Regulatory Affairs or drug development project management
  • Prior experience managing or contributing to a business process
  • Demonstrated experience leading complex, cross-functional initiatives
  • Proven ability to influence without authority
  • Lean Six Sigma certification preferred
  • Experience operating within a Business Process Office preferred

Work Rights

Not specified

Tailored Resume

Cover Letter