×
Register Here to Apply for Jobs or Post Jobs. X

Supplier Quality Engineer

Job in Murrysville, Westmoreland County, Pennsylvania, 15668, USA
Listing for: Katalyst Healthcares & Life Sciences
Full Time position
Listed on 2026-07-19
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below

Job Title

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.
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary