Supplier Quality Engineer

Posted 19 Days Ago
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Manchester, NH, USA
In-Office
Junior
Healthtech • Biotech
The Role
The Supplier Quality Engineer oversees supplier quality activities for new product introductions and sustaining manufacturing in a regulated environment, ensuring compliance with quality standards and managing supplier performance.
Summary Generated by Built In
The Supplier Quality Engineer is responsible for leading supplier quality activities during design transfer and process/product validation. This role ensures supplier compliance to applicable requirements, including 21CFR, ISO 13485, and drives supplier development and performance management processes. The SQE serves as a key technical and quality liaison between the DEKA design team and manufacturing partners with primary responsibility for ensuring suppliers are capable of consistently meeting quality, regulatory, and performance expectations. This role will heavily support process and tool validation support, while also managing sustaining supplier quality performance for production materials and services.
How you will make an impact as a Supplier Quality Engineer:
  • Review and approve supplier documentation including certifications, validations, and quality records
  • Ensure supplier readiness for production launch, including quality systems, and process controls
  • Participate in design transfer and process/tool validation activities such as IQ/OQ/PQ, MSA and Statistical analysis
Sustaining Supplier Quality Management
  • Supplier development and continuous improvement to ensure effective design transfer
  • Monitor supplier performance using quality metrics (e.g., SCARs, defects, delivery performance)
  • Lead/Support supplier corrective action activities (SCAR/CAPA) and ensure timely closure
  • Conduct supplier performance reviews and drive continuous improvement initiatives
  • Support containment, root cause analysis, and resolution of supplier-related quality issues
Supplier Quality System & Compliance
  • Ensure supplier compliance with applicable regulatory and quality system requirements including ISO 13485
  • Support external and internal audits involving supplier quality systems
  • Drive adherence to change notification and supplier control requirements
Cross-Functional Collaboration
  • Partner with Contract Manufacturing, Procurement, and Engineering
  • Support material nonconformance investigations and disposition decisions
  • Provide supplier risk input to project teams and change control processes
  • Support supply continuity and risk mitigation strategies
  • Writing Test Methods to support Validation
Skills you will need to be successful in this role:
  • Bachelor’s degree in Engineering, Life Sciences, or related technical field; or equivalent experience in regulated industry may be considered in lieu of degree.  
  • 3–5 years of experience in Supplier Quality, Quality Engineering, or related role in medical device or regulated industry
  • Strong knowledge of ISO 13485 and medical device regulatory requirements
  • Experience with supplier audits, qualification, and risk-based supplier management
  • Experience supporting NPI or design transfer activities strongly preferred
  • Strong understanding of manufacturing processes, validation, and quality systems.
Skills & Competencies
  • Experience with medical device manufacturing and global supply chains
  • Ability to interpret mechanical drawings
  • Familiarity with statistical tools (Minitab), risk analysis (FMEA), and CAPA systems
  • Experience in process and tool validation
  • Strong technical judgment and problem-solving skills
  • Ability to lead supplier interactions and drive accountability
  • Excellent communication and cross-functional collaboration skills
  • Strong root cause analysis and data-driven decision-making capability
  • Ability to manage multiple priorities in a fast-paced NPI and production environment
  • High attention to detail and regulatory compliance mindset
  • Willingness to travel both domestically and internationally to suppliers as needed, estimated to be 20% travel
Preferred Certifications
  • ISO 13485 Internal Auditor certification preferred.
  • ASQ certifications (Supplier Quality Professional, Green Belt, CQE, CQA, or similar) are a plus.

Skills Required

  • Bachelor's degree in Engineering, Life Sciences, or related technical field
  • 1-3 years of experience in Supplier Quality or Quality Engineering
  • Strong knowledge of ISO 13485 and medical device regulatory requirements
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The Company
HQ: Manchester, NH
670 Employees
Year Founded: 1982

What We Do

DEKA is one of the leading research and development companies in the country and is the birthplace of some of the most innovative and life-changing products of our time. For over thirty years, DEKA Research & Development Corp. has made Manchester, New Hampshire home. Located about an hour from Boston, the beach, and the mountains, we are situated in the beautiful and historic Amoskeag Millyard buildings located in downtown Manchester. DEKA continues to be a place where no idea seems too big and where creativity and crazy cool gizmos reign supreme. The engineers, technicians, machinists, designers and all of the other folks who make up DEKA are some of the most creative and innovative professionals you could ever hope to meet. It's a place where one crazy idea can end up being the next greatest invention. At DEKA we embrace the spirit of innovation and constantly aim to turn the impossible into a reality. DEKA is filled with people who are driven to be among the best and brightest in their field of work. It’s a concentrated bunch of really smart thinkers, doers and problems solvers, who are driven to using innovative design solutions and state-of-the-art technology to improve lives. We all see endless possibilities in the power of technology to do good. Employees have the opportunity to work on diverse projects that have a positive, enduring impact on millions of people worldwide. We are growing! We're always seeking passionate individuals to join our growing team of evolved thinkers.

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