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Salary
$119k – $178k per year
Location
In office (United States)
Seniority
Senior · 10+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Insulet (NASDAQ: PODD), headquartered in Massachusetts, is an innovativemedical device company dedicated to making the lives of people with diabetesand other conditions easier through the use of its Omnipod® System productplatform. The Omnipod® System provides an alternative to traditional insulindelivery methods. With its simple, wearable design, the disposable Podprovides up to three days of non-stop insulin delivery, without the need to seeor handle a needle.

Job Summary

Take the lead in driving manufacturing excellence for Insulet’s innovative Omnipod® platform in a highly automated, high-volume medical device environment. This role offers the opportunity to lead process improvements, equipment validations, new product introductions, and continuous improvement initiatives that directly impact product quality, efficiency, and patient outcomes. Ideal for engineers with strong Lean Six Sigma, statistical analysis, automation troubleshooting, and project management expertise, this position provides the chance to work cross-functionally with Operations, Quality, Controls, and Engineering teams while supporting cutting-edge manufacturing technologies in a fast-growing global organization committed to improving the lives of people with diabetes.

Company Overview

Insulet started in 2000 driven to achieve our mission of enabling our customers to enjoy simplicity, freedom and healthier lives through the use of our Omnipod® product platform. In the last two decades we have improved the lives of hundreds of thousands of patients who have insulin-requiring diabetes, by using innovative technology that is wearable, waterproof, and lifestyle accommodating. We are on an exciting trajectory of significant growth and global expansion enabling us to reach more patients around the globe.

We are looking for highly motivated, performance driven individuals who want to be part of building our Center of Excellence and be at the forefront of our rapidly growing global footprint. We are looking to hire amazing people who are guided by shared values and desire to exceed customer expectations. Our continued success depends on it.

Position Overview

We are seeking a skilled and motivated Senior Manufacturing Engineer to join our dynamic team. The ideal candidate will have experience in a high-volume, highly automated manufacturing environment and will be responsible for ensuring the efficient production of our electro-mechanical medical devices. This role requires a strong background in problem-solving techniques, root cause analysis, lean methodologies, statistical process control, design of experiments (DOE), and validation techniques.

Responsibilities

  • Continuous Improvement: Develop and drive continuous improvement efforts for manufacturing processes and equipment.
  • New Product Introduction: Lead project deliverables for installation of new manufacturing equipment, manufacturing equipment upgrades, and new component introductions.
  • Process Improvement: Drive product and process improvements to support the company's objectives of best quality, highest efficiency, and lowest cost.
  • Key Performance Indicators: Establish, Monitor, and Report on critical performance and process metrics; own the required efforts to ensure these KPIs are at or above target. At all times maintain a cGMP compliant environment and operate within FDA guidelines for Class II Medical Device manufacturing.
  • Root Cause Analysis: Lead and conduct structured root cause investigations using standardized templates and problem-solving tools.
  • Project Management: Manage all project phases from concept, specification, cost justification, project management, installation, training, qualification, implementation into manufacturing, and support.
  • Validation: Develop and execute validation (IQ, OQ, TMV, CSV, PQ) protocols for new and existing processes and equipment. Write validation/qualification reports.
  • Cross-Functional Collaboration: Work closely with Maintenance, Equipment Design, Controls, Operations, and Quality teams to ensure seamless production and continuous improvement.
  • Documentation: Maintain accurate and detailed documentation of processes, experiments, and validation activities per industry GDP practices. Manage all documentation within Insulet Digital Systems (QMS, PLM, PDM).
  • Compliance: Maintain a cGMP compliant environment and operate within FDA and ISO guidelines for Class II Medical Device manufacturing.

Required Skills and Competencies

  • Proficient in all Microsoft Office tools
  • Excellent Microsoft Excel and Data Analysis Skills
  • Working knowledge of Minitab and/or JMP statistical analysis software
  • Working Knowledge of Solidworks and print reading
  • Proficient in Six Sigma/Lean manufacturing concepts
  • Comfortable troubleshooting mechanical equipment both Semi and fully automated
  • Basic knowledge of common challenges with assembly of molded components, stamped metal, and springs
  • Strong command of structured problem-solving tools
  • Strong project management skills

Education and Experience

  • High School diploma and 10+ years of practical experience in Engineering in a highly regulated manufacturing environment (e.g. Medical, Aerospace, Automotive)
  • B.S. in Mechanical/Industrial/Electrical Engineering or equivalent field, and 5+ years of experience.
  • M.S. in Engineering or Engineering Management, with 3+ years of experience.
  • Experience in the medical device industry is preferred. High-Volume Manufacturing and/or Automation Experience is a plus.

Additional Information

  • The position requires on-site working at the Acton site.
  • Up to 5% travel required; Ability to travel internationally (North America and APAC)

NOTE: This position requires on-site working (requires on-site office/plant/lab work). #LI-Onsite

Additional Information:

Compensation & Benefits: For U.S.-based positions only, the annual base salary range for this role is $118,700.00 - $178,025.00 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.

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