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Supplier Quality Engineer

Job in Santa Rosa, Sonoma County, California, 95402, USA
Listing for: SMC Ltd
Full Time position
Listed on 2025-12-02
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
  • Engineering
    Quality Engineering, Process Engineer
Salary/Wage Range or Industry Benchmark: 86000 USD Yearly USD 86000.00 YEAR
Job Description & How to Apply Below

Overview

Supplier Quality Engineer role at SMC Ltd. This role ensures supplier quality at SMC Ltd. by supporting Quality Systems Management and leading strategic auditing, supplier/component development, qualification, and sourcing in collaboration with Procurement, Operations, and Quality. The position is accountable for Supplier Quality Engineering deliverables across new product development, manufacturing launch, and sustaining activities, while driving continuous improvements. Performance is evaluated on execution, adherence to timelines, production support, quality outcomes, communication, continuous improvement, and strong cross-functional collaboration.

Base

pay range

$86,000.00/yr - $/yr

Essential

Job Duties and Responsibilities
  • Plan, conduct, and document supplier audits to ensure compliance with quality standards and regulatory requirements.
  • Manage supplier classification changes/updates and maintain accurate supplier records and information.
  • Open, track, and follow up on Supplier Corrective and Preventive Actions (CAPAs) to drive timely resolution.
  • Collaborate with Quality Engineers on customer complaints related to supplier performance.
  • Provide Supplier Scorecard inputs to support supplier performance monitoring and evaluation.
  • Review, assess, and process supplier change requests in alignment with quality and regulatory requirements and in collaboration with applicable stakeholders.
  • Support supplier selection, classification, and initial evaluations for new and existing suppliers.
  • Manage Supplier PPAPs (Production Part Approval Process), including record creation in IQMS and communication with suppliers and customers.
  • Collaborate in developing/improving receiving inspection instructions/techniques of purchased parts.
  • Lead supplier Qualifications including activities such as supplier Measurement System Analysis (MSA), tolerance and GD&T reviews, FMEA, control plans, FAI and DOE input for purchased components.
  • Provide inputs and collaborate on Advanced Quality Plans (APQP) to ensure robust product launches and process controls.
  • Contribute to the Validation Master Plan for purchased components and services, integrating supplier requirements into the overall validation strategy.
  • Provide Supplier Quality technical support to Program Management Department.
  • Collaborate in Engineering Change orders that impact purchase parts or services.
  • Identify and address opportunities for improvement to supplier related processes.
  • Develops, maintains and updates Procedures, Work Instructions, and Forms.
  • Point of contact for suppliers, internal and external customers for supplier related issues.
  • Supports the ISO 13485 Business Management System through Internal Auditing.
  • Assist with third party and FDA quality audits as needed.
  • Perform other duties as assigned.
Essential Qualifications
  • Bachelor’s degree in Engineering or a related technical discipline.
  • 2–4 years of experience in a Supplier Quality role within the medical device manufacturing industry, with strong knowledge of ISO 13485:2016 and 21 CFR Part 820 requirements.
  • Hands-on experience with Gage R&R, CpK/PpK studies, and Design of Experiments (DoE).
  • Proficiency in validation/qualification activities (IQ, OQ, PQ).
  • Solid knowledge of risk management standards (ISO 14971) and application of risk assessment techniques such as FMEA.
  • Familiarity with quality processes and tools including CAPA, PPAP, Root Cause Analysis, and structured problem-solving methodologies (e.g., 8D, 5 Whys).
  • Experience planning and conducting supplier audits to ensure compliance with quality standards and regulatory requirements.
  • Strong understanding of ISO 13485 quality systems and regulatory expectations under 21 CFR 820.
  • Proficient in Minitab and the Microsoft Office Suite (Excel, Word, PowerPoint, Outlook).
  • Excellent interpersonal, verbal, and written communication skills.
  • Proven ability to prioritize tasks, manage time effectively, and meet deadlines.
  • Detail-oriented, with a strong focus on accuracy, consistency, and quality in deliverables.
  • Ability to read, write, and communicate effectively in English.
Desirable Qualifications
  • Experience with metrology equipment, measurement methods, and inspection…
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