Clinical Program Advisor providing formulary consulting and modeling support for healthcare clients. Utilizing pharmacy expertise to ensure compliance and optimize client outcomes.
DF
Hybrid Director, Program Management – Operations
Posted 3 hours ago
About the role
- Director, Program Management & Operations leading quality initiatives in regulated industries. Engaging with senior leadership and managing strategic programs at Insulet Corporation.
Responsibilities
- Lead and manage a portfolio of strategic regulatory and quality programs, ensuring alignment with enterprise priorities and compliance requirements
- Partner with all functional area VPs and Management staff and other enterprise functions, in establishing overall program goals, scope, resources, and the plans for seamless execution of initiatives
- Help define clear strategic priorities, and project milestones across a matrixed, cross-functional team of key stakeholders
- Act as a trusted liaison between executive leadership and program teams, translating strategic goals into actionable plans
- Establish and maintain operating rhythms for leadership meetings as well as strategic priorities
- Drive adoption of standardized tools and frameworks for program tracking and reporting
- Champion a culture of quality and continuous improvement and operational excellence
- Develop and maintain integrated program plans, timelines, and deliverables across functions
- Identify and implement process enhancements to improve efficiency, compliance, and quality outcomes
- Lead cross-functional initiatives to drive enterprise-wide process improvements
- Support development and accountability to budget and other financial planning deliverables across the function
- Optimize resource utilization and monitor KPIs to assess program health and impact
- Prepare executive-level dashboards and reports to communicate progress and escalate risks
- Serve as primary communications conduit to external partners and internal cross-functional project teams executing project tasks and details
Requirements
- Bachelor’s degree in Engineering, Life Sciences, or related field; advanced degree preferred
- 10+ years of experience in program/project management within regulated industries (medical devices, pharma, biotech)
- Deep understanding of quality systems and industry standards (ISO 13485, FDA QSR, EU MDR, etc.)
- Six Sigma certification and experience desired
- Proven track record of leading cross-functional programs and driving enterprise-wide process improvements
- Strong communication, leadership, and stakeholder management skills
- PMP or similar certification preferred.
Benefits
- Medical, dental, and vision insurance
- 401(k) with company match
- Paid time off (PTO)
- And additional employee wellness programs
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