Supplier Quality Engineer

Katalyst HealthCares and Life Sciences

$85K — $110K *
Healthcare
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering, Technical, or Scientific discipline
  • 8+ years of Supplier Quality experience in the Medical Device industry
  • Strong knowledge of quality systems and supplier quality processes
  • Expertise in regulatory requirements related to the medical device sector
  • Familiarity with PPAP, DFMEA, PFMEA, and Process Validation (IQ/OQ/PQ)
  • Proficient in PLM systems and quality documentation tools

Responsibilities

  • Ensure consistent delivery of quality parts, materials, and services from suppliers
  • Evaluate and onboard suppliers for the Approved Supplier List (ASL)
  • Review and approve key quality documentation such as PPAP and DFMEA
  • Conduct supplier risk assessments and maintain risk profiles
  • Facilitate Supplier Quality Agreements and perform supplier audits
  • Support process validation activities including IQ, OQ, PQ
  • Coordinate evaluation and selection of new suppliers for process changes

Benefits

  • Opportunities for professional development and training
  • Collaborative environment with global quality teams
  • Engagement in cutting-edge projects within the medical device field
Full Job Description
Summary :
We are seeking an experienced Supplier Quality Engineer (SQE) with a strong background in the Medical Device industry to support supplier quality, compliance, and process validation activities.

Roles & Responsibilities :
  • Ensure suppliers consistently deliver quality parts, materials, and services meeting company requirements
  • Evaluate and onboard suppliers into the Approved Supplier List (ASL)
  • Review and approve PPAP documentation, Control Plans, Process Flow Charts, Capability Studies, DFMEA, and PFMEA
  • Conduct supplier risk assessments and maintain supplier risk profiles
  • Facilitate Supplier Quality Agreements and conduct supplier audits
  • Support Process Validation activities (IQ, OQ, PQ), MSA/TMV, and Control Plans
  • Coordinate supplier evaluation and selection activities for new suppliers and process changes
  • Manage documentation within PLM systems and ensure timely approvals and releases
  • Collaborate with global quality teams on Supplier Data Review (SDR) and Supplier Owned Quality (SOQ) initiatives
Education & Experience :
  • Bachelor's degree in Engineering, Technical, or Scientific discipline
  • 8+ years of Supplier Quality experience in the Medical Device industry Strong knowledge of quality systems, supplier quality processes, and regulatory requirements
  • Experience with PPAP, DFMEA, PFMEA, MSA, Risk Management, and Process Validation (IQ/OQ/PQ)
  • Experience working with PLM systems and quality documentation tools

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