Process Quality Engineer

As a Quality Control Engineer, you will play a critical role in ensuring Philips products meet stringent quality, safety, and regulatory standards. You will support complex QC activities, troubleshoot abnormalities in manufacturing, drive validation and documentation excellence, and uphold GLP/GMP requirements while working with limited supervision.

Requirements

• Execute diverse and complex quality control tasks using technical knowledge to address abnormalities in manufacturing processes.
• Assist in resolving complex malfunctions and perform product quality inspection activities within project scope.
• Work independently on routine tasks while escalating issues to supervisors as needed.
• Implement quality control procedures and protocols, ensuring adherence to good laboratory practices (GLP) and good manufacturing practices (GMP).
• Support documentation of regulatory requirements for medical-device manufacturing controls and assist with the laboratory chemical hygiene program.
• Contribute to validation protocols, testing methods, and qualification activities for new products and processes.
• Maintain high accuracy by conducting self-checks and taking ownership of the quality of your work.
• Follow all safety protocols, including safe handling and disposal of hazardous materials, to ensure a safe working environment.
• Participate in planning, prioritization, and continuous learning to strengthen quality and technical capability.

Benefits

• Competitive salary
• Benefits package
• Opportunities for growth and development
• Collaborative and dynamic work environment