Katalyst CRO
Supplier Quality Technician
Skills
1 month ago
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Important information
Contract type:
Freelance / Contract
Location:
New Kensington, PA, USA
Work mode:
Onsite
Published on:
17 September 2026
What they need
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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