Supplier Quality Engineer

Katalyst Healthcares & Life Sciences
  • Murrysville, PA
  • Quick Apply
30+ days ago

Job Description

Job Description:
Support Philips Sleep & Respiratory Care manufacturing transfer activities through supplier qualification, APQP execution, process validation, supplier quality management, and sustaining production support.
Responsibilities:
  • Partner with Development, Manufacturing, Procurement, and Suppliers to assess risks and define Critical-to-Quality (CTQ) requirements.
  • Lead and execute APQP deliverables for supplier onboarding, product transfer, and change management activities.
  • Review and support PFMEA, Control Plans, MSA, SPC, Process Validation, and Line Release activities.
  • Support supplier qualification, supplier audits, supplier performance monitoring, and supplier corrective action programs.
  • Drive disposition and resolution of supplier quality issues using CAPA, SCAR, Client, 8D, and root cause methodologies.
  • Support Design Transfer and Manufacturing Transfer activities from source manufacturing sites to receiving manufacturing facilities.
  • Coordinate IQ/OQ/PQ, TMV, validation builds, and process readiness activities.
  • Work closely with cross-functional teams to ensure compliance with quality and regulatory requirements throughout the transfer lifecycle.
  • Support New Product Introduction (NPI), sustaining engineering, and manufacturing change implementation.

Requirements:

  • 5+ years of Supplier Quality Engineering experience in Medical Devices or other regulated industries.
  • Hands-on experience with APQP, PPAP/SPPA, PFMEA, Control Plans, MSA, SPC, and Process Validation.
  • Strong knowledge of CAPA, SCAR, Client, Root Cause Analysis, and Supplier Quality Systems.
  • Experience supporting Manufacturing Transfer, Design Transfer, or NPI programs.
  • Working knowledge of ISO 13485 and FDA 21 CFR Part 820 requirements.
  • Strong communication and stakeholder management skills.

Preferred Experience:

  • Philips / Philips Respironics experience.
  • Design Transfer or Manufacturing Transfer Lead experience within respiratory, ventilator, CPAP, or sleep therapy device companies.

Numbers & Facts

LocationMurrysville, PA

Skills

  • 8Dunmatched
  • Advanced Product Quality Planning (APQP)unmatched
  • Auditingunmatched
  • Change Managementunmatched
  • Code of Federal Regulationsunmatched
  • Communication Skillsunmatched
  • Corrective Actionunmatched
  • Corrective and Preventative Action (CAPA) Systemsunmatched
  • Cross-Functionalunmatched
  • Engineeringunmatched
  • FDA (Food and Drug Administration)unmatched
  • ISO (International Organization for Standardization)unmatched
  • Leadershipunmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Medical Equipmentunmatched
  • Onboardingunmatched
  • Performance Analysisunmatched
  • Process Failure Mode and Effects Analysis (PFMEA)unmatched
  • Process Validationunmatched
  • Product Supportunmatched
  • Product/Service Launchunmatched
  • Production Part Approval Process (PPAP)unmatched
  • Production Supportunmatched
  • Quality Engineeringunmatched
  • Regulatory Complianceunmatched
  • Regulatory Requirementsunmatched
  • Respiratory Medicineunmatched
  • Respiratory Therapyunmatched
  • Risk Analysisunmatched
  • Root Cause Analysisunmatched
  • Vendor/Supplier Evaluationunmatched
  • Vendor/Supplier Quality Managementunmatched
  • Vendor/Supplier Selectionunmatched
  • Ventilatorunmatched

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