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The Manager of Systems Design Verification will oversee the design verification process for Insulet’s products, managing technical and human resources, planning and executing system level testing, and developing strategies to improve testing efficiency. This role requires leading an engineering team, optimizing testing processes, and ensuring timely project completion while maintaining high technical standards.
The Staff Software Engineer will design, develop, test and document high-quality medical device software for Insulet products, mentor team members, and collaborate with product managers and designers on new features. Responsibilities include enforcing software best practices, ensuring quality in architecture, and exploring new technologies.
The Senior PCB Design Specialist will be responsible for creating and optimizing PCB layouts, maintaining CAD libraries, generating design documentation, and collaborating with engineering teams for low power wearable medical devices. The individual will ensure designs meet manufacturability standards and participate in design reviews while staying current with industry trends.
The Senior Controls Engineer at Insulet is responsible for developing and enhancing control systems for assembly and packaging equipment, leading installations, and driving continuous improvements. This role demands strong analytical skills and the ability to create innovative solutions in dynamic environments.
As a Territory Manager, you will develop and lead business strategies while fostering relationships with healthcare professionals. Your role includes meeting sales targets, managing patient onboarding, and executing field sales initiatives to drive market share growth.
The Systems Engineer V&V will lead verification and validation activities for new product development and sustaining products, develop testing plans and schedules, manage test cases, mentor team members, and ensure compliance with quality and regulatory standards.
The Quality Systems Specialist will support ISO 13485-certified QMS, manage CAPA processes, conduct audits, monitor and analyze quality systems, and ensure compliance with regulatory standards in a medical device company.
The Supplier Engineer will manage root cause investigations, execute assembly validations of new supplier tooling, implement improvement projects, and assist in resolving quality issues related to supplier components. They will establish vendor relationships and lead cross-functional teams towards continuous improvement goals in a factory setting.
The Failure Analysis Engineer will conduct post-market investigations of FDA-approved medical devices, ensuring compliance with quality standards and collaborating with cross-functional teams to perform root cause analysis on failures. Responsibilities include product testing, maintaining quality records, and assisting during regulatory inspections while driving process improvements with Lean Six Sigma methodology.
The Territory Manager is responsible for achieving sales quotas by targeting healthcare professionals and organizations in the diabetes market. Responsibilities include managing client relationships, training customers on products, executing sales strategies, and collaborating with internal teams to ensure profitable sales and market growth.
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