Insulet Corporation

Director

• Drive Insulet’s global pricing vision, strategy, governance, insights, and operational execution across all markets for current and pipeline assets
• Lead the global pricing capability and team, reporting to the VP of Global HEMA
• Design globally led payer and pricing research
• Serve as senior subject-matter expert and internal consultancy resource on pricing research, affordability-driven pricing and access programs, and pricing input for cross-functional projects
• Co-drive global pricing and access principles across markets
• Develop value-based and sustainable global pricing and contracting strategies
• Explore innovative funding, contracting, and pricing arrangements across the product lifecycle
• Assess external developments in pricing regulation, healthcare financing, and cost containment and recommend responses
• Oversee updates to global pricing governance and related processes and resources
• Develop decision-support tools and processes, including pricing databases and pricing business case review templates
• Coordinate pricing analytics, scenario modeling, performance tracking, dashboards, and reports across global markets
• Lead and coach preparation and review of submissions to the Global Pricing Council
• Serve as Secretary of the Global Pricing Council and manage its preparation, agenda, and content
• Lead, coach, and grow the global pricing team and increase pricing acumen across the access community and enterprise
• Travel domestically/internationally, estimated at 20%

Senior Director, Global Head of Pricing

Engineer

• Lead, plan and implement supplier capital and tooling qualifications from project kick-off through implementation into full production
• Own project schedules and assigned budgets, and report status, risks and mitigation plans to stakeholders and leadership
• Partner with R&D, Quality, Automation and Manufacturing teams to deliver design-for-manufacturability analysis and support
• Author or review supplier validation and qualification protocols, and coordinate execution, data analysis and final reporting
• Lead procurement, installation and start-up of manufacturing equipment at global suppliers
• Evaluate and manage prototype suppliers, place purchase orders and manage part deliveries against program timelines
• Investigate supplier quality issues and lead corrective and preventive actions to closure
• Drive results with teams spanning programs, engineering, purchasing and the supply base
• Travel to supplier sites for prototype builds, tooling trials, equipment installation and qualification runs

Senior Project Engineer

Procurement

• Administer Insulet’s purchasing system
• Request onboarding paperwork from suppliers
• Track weekly, monthly, quarterly, and annual supplier performance metrics
• Manage the open order report
• Work with Insulet stakeholders to refine purchasing policies, procedures, and systems
• Coordinate new supplier setup
• Manage and maintain master data information
• Verify purchase requisitions against the master list and clarify unclear items
• Recommend substitute items and alternatives
• Convert requisitions into purchase orders and forward them to suppliers
• Verify purchase order specifications and prices
• Collect, analyze, and summarize purchasing data and trends
• Monitor shipments and trace undelivered goods
• Resolve shipment errors with suppliers
• Expedite orders when necessary
• Negotiate purchasing agreements with suppliers
• Oversee inventory movements, including ordering and receiving
• Perform other duties as required

Procurement Coordinator III

Compliance

• Lead domestic and international regulatory registrations and submissions activities
• Support regulatory approval initiatives for medical devices in domestic and international markets
• Provide regulatory affairs support for product development, manufacturing, and clinical studies, including pre-market, post-market, and physician-initiated studies
• Support ongoing compliance and corporate initiatives
• Partner with Marketing and Development teams on marketed products, labeling, promotional materials, product changes, and documentation requiring government approval
• Compile and submit documentation supporting marketing initiatives
• Review marketing, sales, packaging, and labeling materials for regulatory impact
• Represent Regulatory Affairs on project teams and in meetings involving labeling and promotion decisions
• Assist with pre-market and post-market filings, including 510(k), IDE, PMA, CE Marking, Canadian, EU, and ROW registrations
• Prepare submissions and reports for FDA and other international agencies
• Plan, create, organize, and interpret regulatory documents for submission
• Review and approve specifications, procedures, schedules, test protocols, reports, and validations
• Evaluate and present change assessments to support timely compliance
• Review, evaluate, and approve Engineering Change Orders, especially significant changes and revisions
• Perform other duties as required

Senior Regulatory Affairs Specialist

• Lead, coach, and develop a team of market access professionals
• Develop value propositions, messaging, and resources for field teams to secure access
• Develop materials, publications, and communication strategies to broaden awareness of Insulet and product value among payors in US and global markets
• Build an inventory of commercial insights for government and private payors, pharmacy benefit managers, distribution channel vendors, health benefit professionals, and national employers
• Build strategies for successful post-contracting programs and pull-through strategies
• Create marketing materials addressing payor and employer critical success factors
• Develop coverage strategies for new and potentially acquired products
• Provide input into outcomes trials needed to support value-based reimbursement
• Develop and implement strategies and deliverables to secure access and appropriate reimbursement rates for Insulet innovations
• Collaborate with Marketing, Medical Affairs, Sales, Field Managed Care, and National Account teams
• Report to the Vice President of Market Access

Director, US Pricing

DevOps Engineer

• Monitor CI/CD pipeline runs and investigate basic failures
• Escalate recurring or complex pipeline issues to senior DevOps team members
• Maintain build and deployment documentation, including runbooks, setup steps, and troubleshooting notes
• Assist with access requests, environment checks, release support activities, and tool configuration updates
• Support the design, maintenance, and operation of CI/CD pipelines used to build, package, test, and deploy products
• Help automate repetitive processes and support software release activities
• Contribute to continuous improvement across development teams
• Support development, test, integration, and production environments under senior team guidance

Co-op, DevOps Engineer

Software Engineer

• Design, develop, test, and document embedded system software for new and existing Insulet products
• Ensure software designs comply with company policies and medical-product design and maintenance requirements
• Write and maintain design documentation and testing requirements
• Collaborate with Quality, Regulatory, Marketing, and Manufacturing to meet technical, regulatory, and manufacturing requirements
• Work with software, software QA, and hardware engineers to integrate, debug, and test systems
• Participate in product design reviews
• Contribute to software project initiatives related to product development and improvements
• Perform other duties as required

Product Designer

• Lead and develop a team of UX designers and researchers supporting the Omnipod 5 sustaining portfolio
• Own and continuously improve the UX operating model for the Omnipod 5 sustaining business
• Establish scalable processes for UX intake, prioritization, resource allocation, capacity planning, and roadmap alignment
• Develop and maintain operational frameworks that increase delivery predictability and team effectiveness
• Drive standardization of UX workflows, tools, templates, documentation, and governance
• Create and manage UX performance metrics and dashboards demonstrating operational health and business impact
• Lead continuous improvement initiatives to reduce inefficiencies, rework, and delivery bottlenecks
• Partner with Product Management and Engineering leadership to align UX work with business priorities and release plans
• Manage UX capacity forecasting, quarterly planning, and portfolio prioritization activities
• Facilitate planning discussions balancing customer needs, business value, technical constraints, and regulatory commitments
• Provide visibility into UX resource allocation, dependencies, risks, and delivery forecasts
• Establish governance mechanisms enabling informed decision-making and prioritization
• Define and evolve engagement models between UX and cross-functional partners
• Ensure UX processes and deliverables support medical device quality system requirements
• Partner with Quality and Regulatory Affairs teams to maintain usability, human factors, and design documentation
• Support audits, submissions, post-market activities, and risk mitigation efforts
• Establish repeatable workflows balancing innovation, efficiency, compliance, and customer experience

Manager, UX Design Operations

Manager

• Contribute to the development and lead execution of a global real-world evidence strategy supporting Insulet’s product portfolio and product development
• Serve as a technical expert identifying evidence needs and how research studies and real-world data support product development and commercialization
• Develop, maintain, and expand a portfolio of real-world data research activities
• Generate timely, strategic evidence demonstrating product benefits
• Define research questions, data sources, study designs, and analytical approaches
• Draft and critically appraise study protocols, statistical analysis plans, reports, and manuscripts
• Identify and contact external stakeholders and key opinion leaders for scientific advice and collaboration
• Collaborate with development, commercial, market access, safety, legal, regulatory, and medical affairs teams
• Ensure scientific rigor across research
• Support development and refinement of internal procedures, workflows, and best practices
• Lead and mentor a team and connect with data analytics and clinical research teams
• Provide biostatistical support to prospective clinical trials, including study design, sample size and power calculations, randomization, endpoint definitions, statistical analysis plans, and interpretation/reporting of results
• Communicate results to internal stakeholders and support scientific presentations and publications

Senior Manager, Medical Affairs – Evidence Generation, Data Insights

• Develop and execute sourcing strategies for approximately $50M in indirect spend
• Lead a team of Category Managers and strategic sourcing activities
• Partner with Finance, IT, R&D, Marketing, Logistics, and Global Supply Chain teams
• Drive cost savings, improve supplier performance, manage risk, and ensure reliable service delivery
• Guide functional groups in discovery, contract negotiation, economic value optimization, delivery, cost management, risk mitigation, and scope-of-work development
• Influence stakeholders to achieve business objectives through recommended sourcing strategies
• Manage performance against contract terms and recommend corrective actions
• Develop, implement, and enforce internal spend management procedures
• Develop and implement supplier scorecards covering quality, supply performance, cost improvements, and innovation support
• Bring should-cost modeling capabilities for key indirect spend categories
• Lead contract negotiations and perform first-pass contract reviews
• Lead cross-functional supplier engagement and continuous improvement
• Monitor market trends and identify new technologies and solutions
• Hire, develop, and manage the indirect category team
• Perform other duties as required

Director, Direct Procurement

Network Engineer

• Support and maintain enterprise and manufacturing network infrastructure at the Costa Rica facility
• Install, configure, and maintain network switches, routers, wireless systems, and firewalls
• Monitor network performance, document issues, and escalate as needed
• Support network security measures across the environment
• Troubleshoot and resolve incidents in a timely manner
• Maintain network diagrams, configuration documentation, and asset inventories
• Collaborate with senior engineers on network projects, upgrades, and facility expansions
• Support network reliability for mission-critical manufacturing systems and applications
• Work with OT/Manufacturing Network Engineers on operational technology networking tasks
• Stay informed about evolving networking technologies and industry best practices

• Work hands-on with lab equipment, including oscilloscopes, power analyzers, Instron, pressure transducers, OGP, and high-speed cameras, to identify bugs, troubleshoot, and perform root cause analysis
• Design test procedures, perform custom tests, and analyze data to support qualifications and design enhancements
• Manage project documentation, including protocols, reports, and design history file documentation, and drive team alignment and approvals
• Assist or lead Engineering Change Orders
• Collaborate with systems, software, mechanical, and electrical engineering teams on device reliability, supplier qualification, and new product development projects
• Perform other duties as required

Co-op, Life Cycle Engineering – Systems

• Lead global payer research activities and capture payer perspectives
• Translate payer insights into product development, commercial assessment, and launch planning processes
• Serve as an access champion for the Next Gen Segment across the Insulet Market Access community
• Collaborate with market access stakeholders to implement Next Gen Segment access solutions globally
• Partner with medical, marketing, and product teams to provide access and payer perspectives
• Partner with Global HEOR and Global Pricing on health economic and pricing strategies
• Identify global payer evidence generation needs and study design requirements
• Own generation of Next Gen payer insights for strategic decision-making
• Lead global payer research engagements, including vendor selection, design, execution, and insights generation
• Integrate payer insights into product stage-gate documents and presentations
• Manage external vendors and budgets
• Travel approximately 10%, flexing based on business need
• Report to the Director, Global Health Economics & Market Access for Next Generation Platforms

Global HEMA New Offerings Manager

Program Manager

• Lead strategic product development programs from concept through commercial launch
• Lead cross-functional teams and external development partners
• Manage segment product development and sustaining priorities by defining scope, objectives, goals, and execution plans
• Lead high-value strategic programs from project inception through production and commercial launch
• Provide leadership to Program Managers and work with functional group management to ensure project elements and milestones are met
• Partner with segment leadership to align EPMO activities with strategic goals
• Initiate and lead cross-functional development programs and sustaining activities for relevant products
• Establish product development program goals, scope, resources, and execution plans with functional leaders
• Lead governance and oversight through the Portfolio Decision Team; communicate status and escalate and mitigate risks
• Provide leadership to the Enterprise Program Management Office to align Program Managers and cross-functional initiatives with business strategies
• Direct program teams with accountability for scope, schedule, resources, delivery, and execution
• Serve as overall program leader for large strategic programs when assigned, ensuring on-time and budget-compliant delivery
• Hire, manage, and mentor staff for individual development and leadership
• Provide an unbiased, data-driven perspective on program status and risks
• Perform additional duties as required

Senior Director, Enterprise Program Management

• Lead global sourcing and procurement strategy for packaging materials
• Develop and execute supplier agreements supporting business growth, supplier performance, risk mitigation, and total cost of ownership reduction
• Lead sourcing events, supplier evaluations, competitive bids, benchmarking, and negotiations for packaging materials, components, tooling, specifications, and supplier services
• Partner with Packaging Engineering, Quality, Operations, Supply Planning, and Manufacturing teams to meet quality, regulatory, capacity, service, and cost requirements
• Establish collaborative relationships with packaging suppliers and senior management teams
• Hold suppliers accountable through business reviews, action tracking, scorecards, quality reviews, and corrective action plans
• Ensure packaging material availability, continuity of supply, and reliable production support
• Serve as escalation point for supplier, capacity, service, quality, and shortage-related issues
• Maintain cost reduction, productivity, packaging improvement, supplier consolidation, and specification optimization opportunities
• Drive projects improving gross margin, working capital, service reliability, lead times, packaging utilization, and operational resilience
• Provide cost/benefit analysis, should-cost modeling, supplier performance reporting, and packaging cost analysis
• Identify packaging solutions that reduce waste, improve material efficiency, and support sustainability goals
• Perform other duties and lead projects as required