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Supplier Quality Technician

Job in New Kensington, Westmoreland County, Pennsylvania, 15068, USA
Listing for: Katalyst CRO
Full Time position
Listed on 2026-09-20
Job specializations:
  • Quality Assurance - QA/QC
    Production QC/QA, Quality Engineering, Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
  • Manufacturing / Production
    Production QC/QA, Quality Engineering, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 60000 - 90000 USD Yearly USD 60000.00 90000.00 YEAR
Job Description & How to Apply Below

Job Description Support manufacturing quality, validation, supplier quality, and production transfer activities during execution of the Philips manufacturing transfer program.

Job Description Support manufacturing quality, validation, supplier quality, and production transfer activities during execution of the Philips manufacturing transfer program.
Responsibilities

  • Support manufacturing quality systems and day-to-day quality assurance activities.
  • Assist in execution of validation protocols, production builds, and process verification activities.
  • Support PFMEA updates, process monitoring, inspection activities, and quality documentation.
  • Assist with CAPA, Client, Quality Notifications, and corrective tracking.
  • Support supplier quality and manufacturing engineering teams during transfer and sustaining activities.
  • Perform data collection, analysis, reporting, and documentation required for validation and quality activities.
  • Participate in manufacturing audits, compliance activities, and continuous improvement initiatives.
  • Support production line transfer and design transfer execution activities.
Requirements
  • 2+ years of experience in Manufacturing Quality, Supplier Quality, Process Quality, or Validation.
  • Experience supporting CAPA, Client, audits, and process quality activities.
  • Familiarity with validation activities, documentation, inspection, and quality systems.
  • Ability to work in manufacturing and regulated environments.
Preferred Experience
  • Medical Device manufacturing environment.
  • Experience supporting production transfers, validation execution, or supplier quality activities.
  • Respiratory, ventilator, CPAP, or sleep therapy product experience.
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