Summary : Support manufacturing quality, validation, supplier quality, and production transfer activities during execution of the Philips manufacturing transfer program.
Roles & Responsibilities : - Support manufacturing quality systems and day-to-day quality assurance activities.
- ssist in execution of validation protocols, production builds, and process verification activities.
- Support PFMEA updates, process monitoring, inspection activities, and quality documentation.
- ssist with CAPA, Client, Quality Notifications, and corrective action 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.
Education & Experience - 6+ 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.
- bility to work in manufacturing and regulated environments.
- Medical Device manufacturing environment.
- Experience supporting production transfers, validation execution, or supplier quality activities.
- Respiratory, ventilator, CPAP, or sleep therapy product experience.
