Supplier Quality & Validation Technician

Katalyst CRO; New Kensington (Westmoreland County); On-site; USD 60,000 - 90,000; Full time

Job summary

Katalyst CRO is seeking a Quality Assurance professional to support manufacturing quality, validation, supplier quality, and production transfer activities during the Philips manufacturing transfer program.

This role involves day-to-day quality assurance, execution of validation protocols, CAPA, audits, and documentation, with collaboration across manufacturing and supplier teams in a regulated environment. Experience in medical device manufacturing and transfer projects is preferred.

Qualifications

• 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.

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.

Skills

Manufacturing Quality

Supplier Quality

Process Quality

Validation

Job description

Katalyst CRO is seeking a Quality Assurance professional to support manufacturing quality, validation, supplier quality, and production transfer activities during the Philips manufacturing transfer program.

This role involves day-to-day quality assurance, execution of validation protocols, CAPA, audits, and documentation, with collaboration across manufacturing and supplier teams in a regulated environment. Experience in medical device manufacturing and transfer projects is preferred.