Director, Program Management & Operations (hybrid)

Insulet

Acton, MA, US
Base: $169,700.00 - $254,525.00; bonus/equity: eli...
Hybrid
Program management in regulated industries
Cross-functional team leadership
Regulatory affairs and quality compliance
The Director, Program Management & Operations is a strategic leader responsible for driving operational excellence and accountability across all Quality and Regulatory Affairs initiatives

Job Summary

  • The Director, Program Management & Operations is a strategic leader responsible for driving operational excellence and accountability across all Quality and Regulatory Affairs initiatives.
  • This position offers a hybrid work arrangement with preferred locations in Acton or San Diego and includes a comprehensive benefits package.
  • Insulet Corporation is an innovative medical device company dedicated to simplifying life for people with diabetes through its Omnipod product platform.

Matching Summary

The Director, Program Management & Operations is a strategic leader responsible for driving operational excellence and accountability across all Quality and Regulatory Affairs initiatives.

Salary

Base: $169,700.00 - $254,525.00; Bonus/Equity: Eligible for incentive compensation; Benefits: Medical, dental, vision insurance, 401(k) with company match, PTO, wellness programs

Skills & Requirements

Must-have

  • Program management in regulated industries
  • Cross-functional team leadership
  • Regulatory affairs and quality compliance
  • Enterprise-wide process improvements
  • Operational excellence and continuous improvement
  • Hybrid work arrangement
  • Stakeholder communication and engagement

Nice-to-have

  • Strategic thinking with operational execution
  • Positive change agent with global mindset
  • Culture ambassadorship and inclusion
  • Customer and market orientation
  • Experience with digital program management tools

Key Requirements

  • Bachelor’s degree in Engineering or Life Sciences
  • 10+ years program/project management experience
  • Experience in regulated industries (medical devices, pharma, biotech)
  • Deep understanding of quality systems and industry standards
  • Six Sigma certification desired
  • PMP or similar certification preferred

Work Rights

Not specified

Tailored Resume

Cover Letter