Process Quality Engineer

Join to apply for the Process Quality Engineer role at Philips
.

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.

• 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 GLP and 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.

• Bachelor’s degree in Engineering, Life Sciences, or related technical field.
• At least 4 years relevant experience in manufacturing quality or QC within a regulated environment.
• Solid understanding of GLP, GMP, and core regulatory expectations.
• Hands‑on experience with SPC (Statistical Process Control) and data‑driven process monitoring.
• Proficiency in Minitab for statistical analysis, control charts, capability studies, and trend evaluation.
• Strong statistical analysis skills (e.g., hypothesis testing, regression, Pareto, Cpk/Ppk).
• Working knowledge of CAPA processes, including root cause analysis and corrective/preventive action implementation.
• Ability to create, interpret, and execute Quality Control Plans and Quality Plans aligned with manufacturing and regulatory requirements.
• Familiarity with structured problem‑solving methodologies such as 8D, 5 Why, and fishbone analysis.
• Strong analytical thinking, documentation discipline, and attention to detail.
• Ability to work under limited supervision while communicating effectively and escalating issues when necessary.
• Commitment to safety, compliance, continuous improvement, and maintaining high standards of quality work.

• Process Quality Management
• Data Analysis & Interpretation
• Design for Quality (DFQ)
• CAPA Methodologies
• Regulatory Requirements
• Manufacturing Processes
• Process Monitoring
• Privacy, Safety and Security Risk Assessment
• Technical Documentation
• Process Engineering

For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. This is an onsite role.

We are a health technology company. We built our entire company around the belief that every human matters, and we won’t stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.

Learn more about our purpose, history, and our culture of impact with care here.