Insulet

Director, IT – QMS and R&D Systems (Hybrid)

US - Massachusetts Full time

Position Summary

The Director of IT for Quality & Regulatory Systems is a key member of Insulet’s Corporate Applications team, responsible for leading the strategic planning, implementation, and management of global systems that support Quality Assurance (QMS), Regulatory Affairs, and Post-Market Surveillance and R&D Systems. This role ensures technology solutions are aligned with business objectives, compliant with regulatory standards, and scalable to support Insulet’s continued growth and global expansion.
 

The Director will oversee a portfolio of validated applications, manage a high-performing global team, and collaborate cross-functionally with internal stakeholders and external partners to deliver innovative, efficient, and compliant systems. This role is instrumental in driving digital transformation across regulated business processes and enhancing operational excellence. As Insulet continues to expand its product portfolio and enter new global markets, we anticipate the need to upgrade or replace existing systems to support our strategic growth. The Director of QMS and R&D Systems will be instrumental in shaping and scaling teams to support these transformation initiatives.

This role will actively contribute to vendor evaluation, selection, and the implementation of new technologies that align with our evolving business needs. We are seeking a visionary leader who can help modernize our systems and drive excellence across quality and regulatory functions in a dynamic, fast-paced environment.
 

Key Responsibilities

Strategic Leadership & Business Alignment

  • Partner with business leaders to align IT strategies with R&D, Quality, Regulatory, and Post-Market priorities

  • Translate business needs into actionable technology roadmaps and solutions

  • Serve as a trusted advisor and provide thought leadership on emerging technologies, vendor capabilities, and industry trends

    Application & Program Management
     

  • Oversee the lifecycle of validated systems including QMS platforms (e.g., TrackWise), Veeva systems, Polarion, eDHR, content management, and labeling tools

  • Lead planning, execution, and governance of programs and projects, ensuring timely delivery and compliance

  • Manage risk, scope, and change across initiatives to maintain alignment with business goals
     

Team Leadership & Development

  • Lead and mentor a global team of managers and professionals, fostering a culture of accountability, collaboration, and continuous improvement

  • Drive performance through coaching, feedback, and professional development

  • Promote cross-functional teamwork and knowledge sharing across IT and business units
     

Performance & Compliance

  • Develop and manage KPIs, scorecards, and performance analytics to drive operational efficiency and continuous improvement

  • Ensure systems meet FDA, SOX, and other regulatory requirements, maintaining validated states and audit readiness

  • Champion best practices in system design, governance, and delivery methodologies (Agile, Scrum, Kanban, Waterfall)
     

Stakeholder & Vendor Engagement

  • Build trust-based relationships with business partners through active listening and strategic alignment

  • Manage vendor relationships, contracts, and third-party consultants to ensure quality and value

  • Support IT intake processes and collaborate with Enterprise Architecture, Procurement, and Agile Delivery Office
     

Global Collaboration & Innovation

  • Work with global process owners to develop scalable, region-specific solutions

  • Evaluate third-party tools for feasibility and business impact

  • Contribute to product roadmaps and support geographic expansion strategies


  Financial Oversight

  • Manage OPEX and CAPEX budgets for the team and assigned projects

  • Contribute to long-range planning and resource forecasting at the program level

Qualifications

  • Bachelor’s degree in Computer Science, Information Systems, or related field (Master’s preferred)

  • 10+ years of IT experience, with 5+ years in leadership roles supporting regulated environments as well as managing a team of senior managers or managers

  • International experience is strongly desired

  • Proven expertise in Quality, Regulatory and R&D systems within the medical device or any other regulatory controlled industry.

  • Strong understanding of GxP, validation, and compliance frameworks

  • Exceptional communication, leadership, and stakeholder management skills

  • Experience with Agile and Waterfall methodologies, and global team management

  • Proven knowledge of the software and systems development life cycle.

  • Knowledge of BI or AI platforms is a plus.     
     

Skills/Competencies:

  • Team leadership and management skills.

  • Self-sufficient, flexible, and motivated team player capable leading teams and managing several activities simultaneously.

  • Ability to work in a deadline focused, dynamic environment, and consistently produce deliverables within agreed upon timelines.

  • Ability to analyze problems and develop solutions.

  • Excellent communication, influencing and negotiating skills are critical.

  • Ability to analyze business processes, design process improvements, and train business users on the new processes.

  • Excellent writing skills.  Must have the ability to express strategy, technical knowledge, and processes in easily understood presentations.

  • Positive, results driven, rational, logical, team player.

  • Ability to rapidly learn and take advantage of new concepts, business models, and technologies.

  • Ability to work independently & on multiple projects against deadlines.

  • Experience in the healthcare, pharma or medical device industry a plus.
     

Physical Requirements:

  •  Less than 25% Travel

    NOTE: This position is eligible for hybrid working arrangements and requires on-site work from an Insulet office.

Additional Information:

Compensation & Benefits: For U.S.-based positions only, the annual base salary range for this role is $168,300.00 - $252,450.00 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.