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Supplier Quality Engineer, Plastics (Onsite - Acton, MA)

Insulet Corporation

Acton, MAOnsitePosted 31 days ago$70,400.00 - $105,650.00
Full TimeEntry LevelQuality (QA / QC)Medical Device
Original posting ↗

Summary

The Supplier Quality Engineer is responsible for ensuring supplier governance and governance of related quality systems. The Engineer creates, monitors, and reports on metrics that show the health and capability of the supplier quality system. The individual maintains records and databases needed for those metrics. The Engineer ensures current products and new projects meet quality and regulatory requirements for medical devices. The Engineer interfaces with other Insulet departments as well as suppliers, contractors, and other external parties on issues related to supplier quality, quality management systems, materials, product support and external and internal audit support.

Job description

Responsibilities

  • Responsible for supplier quality engineering (SQE) deliverables to support Plastics category sourcing strategies and continuity of production.
  • Experience in plastic injection molding.
  • Knowledge in mold tool design, material selection, design for manufacturability (DFM), cosmetic criteria definition, and process qualification.
  • Develop and monitor key performance indicators (KPIs) and other metrics.
  • Develop and deploy dashboards and other visualizations required to support metrics.
  • Develop risk management strategies to mitigate product and compliance risks.
  • Lead SQE efforts in sustaining projects to accomplish primary objectives, including cost reduction, capacity increase, dual sourcing, and risk mitigation.
  • Engage partnerships with suppliers (including sub-tiers) and supply chain management (SCM) to drive superior supplier performance and accountability.
  • Experience in supplier selection, supplier production part approval process (PPAP), DOE, process capability analysis, G R&R, control plan, SPC, and inspection procedure development.
  • Experience in supplier performance monitoring and improvement.
  • Lead root cause analysis of supplier-related non-conforming product issues to address and resolve quality concerns via Supplier Corrective Action Report (SCAR).
  • Drive corrective action and supplier improvement activities that directly impact performance for assigned suppliers.
  • Coordinate review, technical assessment, and documentation for supplier change requests.
  • Experience with supplier quality system (QMS), process, and for-cause audits.
  • Ability to set goals with a proactive approach to complete assignments in a timely, effective, and high-quality manner.
  • Ability to work in a team-oriented and fast-paced environment.
  • Excellent communicator for complex problems, execution plan, progress report out, and escalation to supplier quality leadership and all levels in the organization.

Required Leadership/Interpersonal Skills & Behaviors

  • Demonstrates agility and responsiveness to evolving quality challenges.
  • Effectively influences internal cross-functional teams and external suppliers to drive resolution and improvements.
  • Demonstrates a strong customer-centric mindset.
  • Builds strong cross-functional partnerships across Engineering, Operations, and Account Management.
  • Excellent analytical capabilities and problem-solving skills.
  • Communicates clearly, concisely, and persuasively across all organizational levels.
  • Possess exceptional skill in handling competing priorities and requirements, especially with external entities.
  • Adept at driving consensus and action, culminating in clear communication.
  • Ability to work in a team-oriented, high energy, and fast-paced environment.

Required Skills and Competencies

  • Strong understanding of QMS systems, complaint handling, and regulatory framework (21 CFR Part 820 and Part 11 standard).
  • Exceptional organizational skills and attention to detail.
  • Excellent written and verbal communication abilities.
  • Professional handling of confidential and sensitive information.
  • Proficiency in analyzing quality data and generating actionable insights through dashboards or reports.

Education and Experience

  • Bachelor’s degree in Mechanical Engineering, Industrial Engineering or a related field.
  • 1-3 years of progressive work experience in medical device supplier quality, quality, manufacturing, or engineering.
  • Prior co-op or internship experience is preferred.
  • Experience with plastics manufacturing or materials is a strong plus.

Additional Information

This position is based at our Acton, MA site. Estimated travel: ~25%, with flexibility based on business needs. NOTE: This position requires on-site working (requires on-site office/plant/lab work). #LI-Onsite

Requirements

  • Bachelor’s degree in Mechanical Engineering, Industrial Engineering or a related field.
  • 1-3 years of progressive work experience in medical device supplier quality, quality, manufacturing, or engineering.
  • Experience in plastic injection molding.
  • Knowledge in mold tool design, material selection, design for manufacturability (DFM), cosmetic criteria definition, and process qualification.
  • Experience in supplier selection, supplier production part approval process (PPAP), DOE, process capability analysis, G R&R, control plan, SPC, and inspection procedure development.
  • Experience in supplier performance monitoring and improvement.
  • Strong understanding of QMS systems, complaint handling, and regulatory framework (21 CFR Part 820 and Part 11 standard).
  • Proficiency in analyzing quality data and generating actionable insights through dashboards or reports.
  • Excellent written and verbal communication abilities.
  • Exceptional organizational skills and attention to detail.
  • Ability to work in a team-oriented and fast-paced environment.

Benefits

  • Medical, Dental & Vision
  • 401(k) Matching
  • Paid Time Off
  • Employee Wellness Programs

Company overview

Insulet Corporation (NASDAQ: PODD) is an innovative medical device company headquartered in Acton, Massachusetts, founded in 2000 with a mission to improve the lives of people with diabetes. The company specializes in developing, manufacturing, and marketing the revolutionary Omnipod Insulin Management System, which provides a unique alternative to traditional insulin delivery methods. The Omnipod system features a tubeless, disposable wearable Pod that delivers up to three days of continuous insulin without the need for needles or tubing. Insulet's flagship product, the Omnipod 5 Automated Insulin Delivery System, integrates with continuous glucose monitors to manage blood sugar levels automatically, eliminating multiple daily injections and fingersticks. With operations spanning 25 countries across North America, Europe, the Middle East, and Asia Pacific, Insulet has established itself as a global leader in diabetes management technology. The company employs between 1,001-5,000 professionals dedicated to advancing diabetes care through innovative medical device solutions.

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