Senior Manufacturing Engineer (Onsite - Acton, MA)
About The Position
This Senior Manufacturing Engineer role is responsible for supporting both new manufacturing line/equipment implementation and continuous improvement of existing production processes for Insulet’s Omnipod products. The position focuses on driving manufacturing excellence through improved quality, efficiency, and cost reduction while leading equipment validation, troubleshooting, root cause investigations, and process optimization activities. Working closely with suppliers, contract manufacturers, and cross-functional teams, the engineer will manage projects from concept through production, monitor key performance metrics such as yield and equipment uptime, and ensure compliance with medical device quality and regulatory requirements. The ideal candidate has a strong engineering background, experience in medical device manufacturing, expertise in automation and process improvement, and a passion for solving complex manufacturing challenges in a highly regulated environment.
Requirements
- 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
- BS. in Mechanical/Industrial/Electrical Engineering and 6+ years of medical device experience; preferably in a manufacturing environment
- MS. in Mechanical/Industrial/Electrical or Engineering Management with 5+ years of medical device experience; preferably in a manufacturing environment
Nice To Haves
- Decision Making – has a systematic and methodical approach to making decisions, seeks out and explores relevant information, thinks creatively beyond the immediate problem, assimilates facts quickly, challenges assumptions, and considers business implications of potential solutions.
- Communication Skills – Conveys information effectively, actively listens, resolves conflict constructively.
- Work Organization – Takes a structured, economical approach to resources including time, people, money, and equipment.
- Problem Solving – Uses a systematic, methodical approach to gather facts, define problems, generate and implement solutions.
- Initiative – Makes decisions and takes actions appropriately. Willing to take risks as circumstances require.
- Planning Skills – Sets goals and priorities, thinks ahead, identifies activities and resources needed to achieve goals.
- Perseverance – Achieves objectives by overcoming difficulties through tenacity and resilience.
Responsibilities
- Drive product and process improvements in support of Insulet’s Operations (3) main objectives Best Quality Highest Efficiency Lowest cost
- Project deliverables for installation of new manufacturing equipment and manufacturing equipment upgrades
- Support equipment validation and continuous improvement activities at Insulet manufacturing facilities
- Support responsibility for all project phases from concept, specification, cost justification, project management, installation, training, qualification, implementation into manufacturing, and support.
- Monitor and report on yield and equipment up-time information; own the required efforts to ensure these KPIs are at or above target
- Develop and drive Continuous improvement efforts.
- Generate validation/qualification (IQ, OQ, TMV, CSV, PQ) protocols, coordinate the execution of the validation/qualification protocols and write validation/qualification final reports
- Possesses strong mechanical analysis skills
- Analyze a product using mechanical engineering methods such as FBD analysis and fundamental physics.
- Use standardized root cause investigation templates and problem-solving tools to carry out non-conforming material investigations
- Implement corrective and preventive actions
- Support new product introduction initiatives
- Travel to key suppliers to help them carry out critical investigations or improvement projects
- Carry out duties in a quality system environment
- At all times maintain a cGMP compliant environment and operate within FDA guidelines for Class II Medical Device manufacturing.
- Author and implement Engineering Change Orders
- Up to 5% travel required, ability to travel internationally
- Performs other duties as required
Benefits
- Medical, dental, and vision insurance
- 401(k) with company match
- Paid time off (PTO)
- And additional employee wellness programs
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What This Job Offers
Job Type
Full-time
Career Level
Senior
