Senior Supplier Quality Engineer

Katalyst HealthCares and Life Sciences

$100K — $120K *
Manufacturing & Automotive
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a related technical field such as Mechanical, Industrial, Manufacturing, or Quality Engineering.
  • 6+ years of experience in Supplier Quality or Quality Engineering.
  • Strong expertise in supplier audits, SCAR, CAPA, and root-cause analysis.
  • Proven track record in supplier qualification and performance management.
  • Comprehensive understanding of quality systems and manufacturing processes.
  • Experience with quality tools such as FMEA, SPC, and MSA.
  • Strong analytical and problem-solving skills.

Responsibilities

  • Lead the supplier qualification, evaluation, and approval process.
  • Develop and enforce supplier quality requirements and specifications.
  • Conduct audits, assessments, and process reviews with suppliers.
  • Drive corrective and preventive actions in SCAR/CAPA activities.
  • Utilize root-cause analysis to investigate nonconformances and defects.
  • Monitor supplier performance metrics and quality indicators.
  • Collaborate with suppliers to enhance processes and reduce defects.

Benefits

  • Comprehensive health and wellness plans including medical, dental, and vision.
  • 401(k) retirement plan with company match.
  • Opportunities for professional development and certifications.
  • Flexible working arrangements and a supportive work environment.
Full Job Description
Job Summary:
The Senior Supplier Quality Engineer is responsible for managing and improving supplier quality performance across the supply chain. This role works closely with suppliers, Engineering, Manufacturing, Quality, Procurement, and Operations teams to ensure purchased materials, components, and services meet established quality and regulatory requirements.
Key Responsibilities:
  • Lead supplier qualification, evaluation, and approval activities.
  • Develop and maintain supplier quality requirements, specifications, and quality agreements.
  • Conduct and support supplier audits, assessments, and process reviews.
  • Lead supplier SCAR/CAPA activities and drive timely corrective and preventive actions.
  • Investigate supplier-related nonconformances, defects, and quality issues using root-cause analysis.
  • Monitor supplier performance using quality metrics, scorecards, PPM, defect rates, and delivery performance.
  • Partner with suppliers to implement process improvements and defect-reduction initiatives.
  • Support PPAP, APQP, FAI, inspection plans, and process validation activities as applicable.
  • Review supplier engineering changes and assess their potential quality and regulatory impact.
  • Support incoming inspection requirements and disposition of supplier-related material issues.
  • Collaborate with Engineering, Manufacturing, Procurement, Quality, and Regulatory teams on supplier quality issues.
  • Provide technical guidance to suppliers on quality system and process requirements.
  • Support internal, customer, and regulatory audits related to supplier quality.
  • Identify supplier risks and develop appropriate mitigation and continuous improvement strategies.

Requirements:
  • Bachelor's degree in Mechanical Engineering, Industrial Engineering, Manufacturing Engineering, Quality Engineering, or a related technical field.
  • 6+ years of experience in Supplier Quality, Quality Engineering, Manufacturing Quality, or a related discipline.
  • Strong experience with supplier audits, SCAR, CAPA, RCA, and nonconformance management.
  • Experience with supplier qualification and performance management.
  • Strong understanding of quality systems and manufacturing processes.
  • Experience with FMEA, SPC, MSA, control plans, and process capability.
  • Knowledge of PPAP, APQP, First Article Inspection (FAI), and supplier development.
  • Experience working with cross-functional engineering, manufacturing, procurement, and quality teams.
  • Strong analytical, problem-solving, communication, and project-management skills.

Preferred Qualifications:
  • Experience in medical device, pharmaceutical, aerospace, automotive, or other regulated manufacturing.
  • Knowledge of ISO 13485, ISO 9001, FDA 21 CFR Part 820/QMSR, or applicable industry standards.
  • SQ Certified Quality Engineer (CQE) or Certified Supplier Quality Professional certification.
  • Lean Six Sigma Green Belt or Black Belt certification.
  • Experience with SAP, Oracle, TrackWise, Veeva, ETQ, or other QMS/ERP systems.
  • Experience with machining, injection molding, plastics, electronics, metal fabrication, or other complex manufacturing processes.

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