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Supplier Quality Engineer

Job in South Plainfield, Middlesex County, New Jersey, 07080, USA
Listing for: Katalyst Healthcares & Life Sciences
Full Time position
Listed on 2026-03-03
Job specializations:
  • Engineering
    Quality Engineering, Process Engineer
  • Quality Assurance - QA/QC
    Quality Engineering
Job Description & How to Apply Below

Job Summary:

  • We are seeking a highly skilled and detail-oriented Supplier Quality Engineer to join our team.
  • The ideal candidate will have a strong background in medical device supplier quality, with hands-on experience in supplier qualification, PPAP documentation, and process validation.
  • This role is critical in ensuring that suppliers meet Healthcare's quality standards and regulatory requirements.
Roles & Responsibilities:
  • Supplier Qualification & Management:
  • Qualify suppliers in accordance with company standards.
  • Manage and maintain the Approved Supplier List (ASL) in compliance with Healthcare's purchasing control procedures.
  • PPAP Documentation & Execution:
  • Manage and release all PPAP deliverables including Control Plans, MSA, PFMEA, FAI, etc., within the document control system.
  • Support PPAP execution with suppliers and ensure robust process qualification/validation using IQ, OQ, and PQ methodologies.
  • Define Receiving Inspection requirements.
  • Validate test methods in alignment with internal Healthcare procedures.
  • Cross-Functional Collaboration:
  • Work with cross-functional teams to develop and implement product acceptance sampling strategies.
  • Deploy supplier quality tools such as PFMEA, MSA, control plans for both new and legacy products.
  • Provide technical assistance to suppliers throughout the product/process qualification lifecycle.
  • Ensure delivery of high-quality parts, materials, and services to prevent defects and support client's commitment to reliability.
  • Collaborate with suppliers to address SCAPA/Client issues in compliance with company standards.
Education & Experience:
  • Bachelor's degree in engineering or related field.
  • Minimum 4+ years of experience in supplier quality engineering within the medical device industry.
  • ISO 13485 Certified Talent preferred by client.
  • Strong knowledge of PPAP, IQ/OQ/PQ, PFMEA, MSA, and control plans.
  • Familiarity with FDA and ISO 13485 standards.
  • Excellent communication and problem-solving skills.
  • Ability to work independently and in cross-functional teams.
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