×
Register Here to Apply for Jobs or Post Jobs. X

Quality Engineer

Job in Brockton, Plymouth County, Massachusetts, 02411, USA
Listing for: Stevenson Search Partners
Full Time position
Listed on 2026-09-02
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
  • Engineering
    Quality Engineering, Process Engineer
Salary/Wage Range or Industry Benchmark: 110000 - 160000 USD Yearly USD 110000.00 160000.00 YEAR
Job Description & How to Apply Below

Our On-Demand Talent Solutions team is excited to announce that we are hiring a Senior
Supplier Quality Engineer of Plastics on behalf of our valued client. This client has improved the lives of patients who have insulin-requiring diabetes by using innovative technology that is wearable, waterproof, and lifestyle accommodating.

The Senior Supplier Quality Engineer – Plastics will be responsible for supporting Plastics and Silicone Supplier Quality function while providing both technical ownership across a global supplier network. For supplier quality governance, supplier performance management, quality systems oversight, and execution of strategic initiatives supporting new product introduction, manufacturing expansion, supply continuity, and regulatory compliance.

Responsibilities
  • Own supplier quality deliverables supporting Plastics category sourcing strategies, supplier governance, business growth, manufacturing expansion, dual sourcing, and continuity of production.
  • Demonstrate strong technical expertise in Plastics manufacturing processes and supplier quality systems, including injection molding, tooling and mold design, polymer materials, resin handling and drying, automated assembly operations, process validation, dimensional and functional inspection, SPC, and product reliability testing.
  • Lead supplier selection, qualification, and development activities and drive continuous improvement through supplier scorecards, performance reviews, quality improvement plans, and corrective action programs.
  • Monitor supplier performance and drive measurable improvements in quality, responsiveness, delivery performance, and process capability, while proactively identifying and mitigating product, supplier, operational, and compliance risks.
  • Lead supplier quality system assessments, process audits, surveillance audits, and for-cause investigations, ensuring compliance with corporate quality systems, medical device regulations, industry standards, and supplier quality requirements.
  • Review and approve supplier qualification documentation, process validations, quality plans, inspection strategies, change notifications, and supplier change requests.
  • Lead root cause investigations and Supplier Corrective Action Requests (SCARs), containment activities, effectiveness monitoring, and sustainable corrective actions; serve as escalation point for critical supplier quality issues and compliance risks.
  • Partner with Engineering, Operations, Procurement, Supply Chain Management, Supplier Development, and suppliers to improve process capability and manufacturing performance and support new product introductions, supplier transfers, capacity expansion, and manufacturing readiness initiatives.
Qualifications
  • Bachelor’s degree in Plastics Engineering, Mechanical Engineering, Biomedical Engineering, or related technical discipline; 5–8 years of progressive experience with a bachelor’s degree or 3 years with a master’s degree in medical device Supplier Quality Engineering, Quality Engineering, or Manufacturing Engineering.
  • At least 2 years of demonstrated technical, project, team leadership, or people management experience
    , including supplier performance improvement initiatives and cross-functional quality programs; strong communication and project management capabilities.
  • Comprehensive understanding of plastics manufacturing technologies
    , including injection molding, extrusion, polymer component production, tooling and mold maintenance, automated assembly operations, secondary manufacturing processes, and plastic component suppliers.
  • Strong understanding of Quality Management Systems (QMS), supplier quality systems, supplier qualification, audits, risk management, and regulatory frameworks, including 21 CFR Part 820, 21 CFR Part 11, and IPC-A-610 standards.
  • Expertise in PPAP, DOE, Process Capability Analysis, Gage R&R, Control Plans, SPC, Failure Analysis, Inspection Methodologies, problem-solving methodologies, and continuous improvement techniques.
  • Experience working within regulated industries such as medical devices, pharmaceuticals, aerospace, or other highly regulated manufacturing environments; global supplier quality experience and ASQ CQE, CQA, Six Sigma Green Belt/Black Belt, or equivalent certification preferred.
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary