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.
• This role collaborates with GRA leadership, cross-functional teams, and cross‑enterprise stakeholders to facilitate the identification, design, implementation, and monitoring of scalable, compliant, and efficient regulatory processes.
• 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.

Matching Summary

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

Key Requirements

• 7+ years of experience in pharmaceutical and/or biotech industry
• 4+ years of experience in Regulatory Affairs or drug development project management
• Lean Six Sigma certification preferred
• Bachelor’s degree in Life Sciences, Business Administration, or related field

Work Rights