Senior Director, Quality & Regulatory Strategy & Operations
Reporting to: SVP, Chief Quality, Regulatory, and Compliance Officer
Location: Acton, MA
Role Overview
The Senior Director, Quality & Regulatory Strategy & Operations is a trusted strategic advisor and execution leader to the SVP - Chief Quality, Regulatory, and Compliance Officer (CQRCO). This role partners closely with the Quality, Regulatory, and Compliance Leadership Team, and cross‑functional leaders to define, operationalize, and deliver the enterprise Quality and Regulatory strategy.
Operating at the intersection of strategy, governance, and execution, this leader serves as the Chief of Staff to the CQRCO while also owning program and portfolio management for critical Quality, Regulatory, and Compliance initiatives. The role ensures strategic priorities are clearly defined, resourced, sequenced, and executed with rigor and transparency across the enterprise.
This is a highly visible, enterprise-facing role requiring strong strategic thinking, executive presence, systems leadership, and the ability to drive complex, multi-year transformation initiatives in a highly regulated medical device / healthcare environment.
Key Objectives
Serve as a strategic thought partner and Chief of Staff to the SVP, CQRCO
Translate Quality, Regulatory, and Compliance vision into clear enterprise strategy and execution roadmaps
Establish governance, operating cadence, and program management discipline across Quality & Regulatory initiatives
Drive cross-functional alignment and execution of high‑priority, enterprise‑critical programs
Enable executive decision-making through insightful analysis, scenario planning, and performance tracking
Support organizational readiness for regulatory inspections, audits, and major external milestones
Strengthen integration and coordination across Quality, Regulatory, Compliance, R&D, Manufacturing, Supply Chain, and Commercial teams
Key Responsibilities
Strategy & Enterprise Planning
Partner with the CQRCO and senior leaders to define and articulate the long-term Quality, Regulatory, and Compliance strategy, aligned to corporate objectives and growth plans
Lead development of the annual Quality & Regulatory strategic plan, including prioritization, sequencing, and resourcing of initiatives
Conduct ongoing enterprise landscape assessments, including regulatory trends, enforcement themes, industry benchmarks, and emerging risks
Lead scenario planning and strategic analyses to inform executive decisions related to compliance posture, risk mitigation, and growth-enabling strategies
Chief of Staff to the CQRCO
Act as the CQRCO’s primary strategic and operational integrator, ensuring clarity, focus, and follow‑through across priorities
Prepare executive briefings, strategic updates, and materials for ELT, Board, and external stakeholder engagements
Drive leadership meeting agendas, decision forums, operating cadence, and follow-up actions to ensure accountability
Facilitate communication and alignment across the Quality, Regulatory, and Compliance leadership team and the broader enterprise
Program & Portfolio Management
Establish and oversee a portfolio management framework for Quality, Regulatory, and Compliance initiatives
Lead execution of enterprise‑critical programs, including quality system transformations, regulatory readiness, remediation efforts, inspection preparedness, and capability buildouts
Implement consistent program management standards, milestones, risk tracking, and dependency management
Proactively identify delivery risks, constraints, and gaps; drive mitigation plans and escalation as needed
Cross-Functional Execution & Influence
Serve as a connector across functions, aligning Quality & Regulatory priorities with R&D, Operations, Manufacturing, Supply Chain, IT, and Commercial partners
Lead and influence without direct authority, mobilizing cross‑functional teams to drive outcomes
Support change management and adoption of new processes, systems, and ways of working
Ensure learnings from audits, inspections, and external feedback are translated into sustainable enterprise improvements
Governance, Metrics & Reporting
Define and monitor enterprise-level KPIs related to Quality, Regulatory, and Compliance effectiveness
Develop executive dashboards and performance reporting to support transparency and decision-making
Support preparation for Board-level reviews, external audits, and regulatory engagements
Candidate Profile
The ideal candidate is a high‑caliber strategic leader with deep understanding of Quality, Regulatory, and Compliance within a regulated healthcare environment. They bring a calm, structured, and highly credible presence, thrive in ambiguity, and are energized by shaping strategy and ensuring flawless execution.
This leader is equally comfortable thinking strategically and operating tactically, serving as a trusted advisor to senior executives while driving disciplined execution across large, complex initiatives. They are collaborative, low‑ego, and naturally effective at influencing across boundaries.
Experience & Qualifications
Bachelor’s degree required; advanced degree (MBA, MS, PhD, JD) strongly preferred
12+ years of progressive experience in Quality, Regulatory Affairs, Compliance, Strategy, PMO, or Management Consulting
Demonstrated experience supporting or partnering with C‑suite or senior executive leaders in a Chief of Staff, strategy, or enterprise PMO capacity
Deep understanding of FDA regulations, global regulatory frameworks, quality systems, and inspection readiness
Proven track record leading complex, cross‑functional enterprise programs with material business impact
Strong analytical capabilities, with the ability to synthesize complex data into clear executive insights
Exceptional communication skills (written, verbal, executive presence)
Core Leadership Competencies
Setting Strategy
Articulates a clear, compelling vision that integrates Quality, Regulatory, and Compliance into enterprise value creation
Applies data, insight, and judgment to shape priorities and inform decisions
Balances ambition with practicality, ensuring strategies are executable and sustainable
Executing for Results
Drives disciplined execution with clear accountability, milestones, and outcomes
Navigates ambiguity with confidence and adaptability
Anticipates risks and enables proactive mitigation
Leading Through Influence
Builds trust rapidly across diverse stakeholders
Leads complex initiatives without formal authority
Fosters collaboration, alignment, and shared ownership
Integrity & Judgment
Demonstrates sound judgment, transparency, and ethical leadership
Operates with a strong enterprise mindset, balancing risk, compliance, and growth
NOTE: This position is eligible for hybrid working arrangements and requires on-site work from an Insulet office. #LI-Hybrid
Additional Information:
Compensation & Benefits: For U.S.-based positions only, the annual base salary range for this role is $198,200.00 - $297,350.00 This position may also be eligible for incentive compensation. We offer a comprehensive benefits package, including: • Medical, dental, and vision insurance • 401(k) with company match • Paid time off (PTO) • And additional employee wellness programs Application Details: This job posting will remain open until the position is filled. To apply, please visit the Insulet Careers site and submit your application online. Actual pay depends on skills, experience, and education.Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet’s flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com.
We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!
At Insulet Corporation all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.