Jobs at Insulet

Software Test Engineer responsible for manual and automated testing of software products and iOS applications. Designs test plans, develops automation frameworks and test cases, executes validation, tracks defects, and generates reports. Collaborates with Development, QA, and IT throughout the software lifecycle to ensure requirements, quality, regulatory, and user needs are met. The role also supports requirements reviews, testability improvements, software tool validation, configuration management, and continuous improvement within an Agile development environment.

Develops and executes manual and automated software tests for medical device products, including iOS applications. Creates test plans, test cases, frameworks, use cases, and reports; maintains automated validation databases; identifies defects and collaborates with development, QA, and IT teams. Supports software verification, validation, traceability, code analysis, configuration management, and testing tool validation throughout the product lifecycle.

Owns and scales Insulet’s analytics and BI data product portfolio, including dashboards, datasets, applications, monitoring, and alerting. Partners with stakeholders, data scientists, engineers, and IT teams on data sources, governance, validation, documentation, and ad hoc insights. Manages analytics intake workflows, administers BI tools, supports compliance, and mentors junior analytics engineers.

Manage packaging procurement strategy, supplier sourcing, negotiations, performance, risk, compliance, and cost reduction for manufacturing sites in Malaysia and China. Partner with Engineering, Operations, Quality, and Finance on product introductions, packaging changes, capacity expansion, budgeting, and supplier corrective actions. Track category metrics and ensure reliable, compliant packaging supply while driving continuous improvement.

Leads the design, specification, procurement, installation, commissioning, validation, and continuous improvement of automated assembly and packaging equipment for medical device manufacturing. Coordinates vendors and cross-functional teams, manages technology transfers and capital projects, oversees IQ/OQ/PQ, FAT, and SAT activities, supports capacity expansion, and mentors engineering teams across global sites.

Processes invoices and accounts payable transactions accurately and timely. Reviews documentation and approvals, prepares and distributes checks, handles garnishments, responds to vendor inquiries, maintains AP records and reports, supports month-end closing, and assists with account analysis and finance projects.

Provides business-oriented legal advice, drafts and negotiates commercial agreements, supports contract management and risk assessment, and advises procurement teams. Maintains contract databases, improves legal processes, updates policies and compliance programs, and collaborates on cross-border matters with international legal teams. The role requires a licensed Mexican attorney with 2–4 years of legal experience, fluent English, commercial contracting expertise, and strong analytical and communication skills. Occasional travel and on-site attendance three days weekly are required.

Supports systems engineering for wearable medical devices across the product development lifecycle. Responsibilities include requirements documentation, design verification, troubleshooting, engineering change orders, feasibility testing, technical reviews, device integration, test protocols, and design control documentation. Works with R&D teams to support FDA and international clearance and commercial releases.

Supports the Legal and U.S.-based paralegal teams with end-to-end contract lifecycle administration, including intake, workflow routing, approvals, execution, repository management, renewals, reporting, and compliance tracking. The role also manages legal team requests, identifies process gaps, escalates legal risks, improves CLM workflows, and supports Procurement and cross-functional initiatives. It requires contract administration or legal operations experience, advanced English, strong organizational skills, and proficiency with Microsoft Office and CLM-related tools.

Own the Knowledge Management product vision, roadmap, governance, lifecycle, quality, and continuous improvement. Establish taxonomy, metadata, content standards, localization practices, and audit controls. Partner with platform teams to enable AI, search, virtual agent, and automation capabilities. Track KPIs such as self-service adoption, content usage, quality, and search effectiveness, using data to identify gaps and improve knowledge performance.

Leads and executes risk-based internal audits across global operations, covering planning, testing, reporting, remediation, SOX compliance, governance, risk management, and internal controls. Identifies process and control gaps, assesses regulatory compliance, communicates findings, supports advisory projects and emerging-risk assessments, and recommends business improvements. The role also contributes to audit governance, continuous improvement, stakeholder relationships, and mentoring junior team members.

Leads global and site manufacturing engineering for regulated, high-volume medical-device production. Builds multidisciplinary teams, supports greenfield start-up and scale-up, and oversees equipment design, commissioning, qualification, validation, automation, maintenance, reliability, and continuous improvement. Owns engineering strategy, budgets, resources, KPIs, compliance, supplier coordination, and technical risk. Requires strong cross-functional leadership, manufacturing start-up experience, and expertise in Lean, Six Sigma, process capability, asset management, and regulated quality systems.

The Asia Governance Lead manages project portfolios and governance processes across suppliers, engineering, quality, sourcing, and manufacturing teams. Responsibilities include tracking project status and risks, maintaining governance data, creating dashboards and leadership updates, improving workflows and reporting, training project leads, and driving consistent standards across the Asia portfolio. The role supports capital tooling and equipment projects, financial and resource management, supplier projects from concept through production, and global governance alignment. Travel of approximately 10% to 25% is required.

Design, install, troubleshoot, and program control systems, PLCs, HMIs, SCADA, vision systems, drives, and robotics for high-speed manufacturing. Lead continuous improvement, develop control programs, analyze data, support cGMP compliance, and coach others on machine and vision programming.