Process Quality Engineer

Job Title

Job Description

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.

Your role:

• 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.

• Aids to implement quality control procedures and protocols ensuring adherence to good laboratory practices (GLP) and good manufacturing practices (GMP).

• Support documentation of regulatory requirements for medicaldevice 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 selfchecks 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.

Youre the right fit if you have:

• Bachelors degree in Engineering Life Sciences or related technical field.

• Atleast 4 years relevant experience in manufacturing quality or QC within a regulated environment

• Solid understanding of GLP GMP and core regulatory expectations.

• Handson experience with SPC (Statistical Process Control) and datadriven 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 problemsolving 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.

Preferred Skills:
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

How we work together
We believe that we are better together than apart. For our office-based teams this means working in-person at least 3 days per week.
Onsite roles require full-time presence in the companys facilities.
Field roles are most effectively done outside of the companys main facilities generally at the customers or suppliers locations.
This is an onsite role.

About Philips
We are a health technology company. We built our entire company around the belief that every human matters and we wont 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 business.
Discover our rich and exciting history.
Learn more about our purpose.
If youre interested in this role and have many but not all of the experiences needed we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here.