Process Quality Engineer at Philips

Batam, Riau Islands, Indonesia -

Full Time

Start Date

Immediate

Expiry Date

26 Mar, 26

Salary

0.0

Posted On

26 Dec, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Control, GLP, GMP, Statistical Process Control, Minitab, Data Analysis, CAPA, Root Cause Analysis, Quality Control Plans, Problem Solving, Analytical Thinking, Documentation Discipline, Attention to Detail, Continuous Improvement, Manufacturing Processes, Process Monitoring

Industry

Hospitals and Health Care

Description

Job Title Process Quality Engineer 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 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. You're the right fit if you have: Bachelor’s 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. 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. 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 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. About Philips 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 business. • Discover our rich and exciting history. • Learn more about our purpose. If you’re 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. At Philips, we believe that every human matters. As a global health-tech leader, we focus on improving people’s health and wellbeing through meaningful innovation. The people who work here share our passion and are motivated to bring this purpose to life. For more than 130 years, we have been creating technologies and innovations that improve people's lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health. Together, we deliver better care for more people because we believe that every human matters. That's why we're taking steps to create an environment where we acknowledge and embrace our differences and uniqueness and listen to and value each other's views. When people feel cared for and listened to, they bring their best qualities to work, leading to better collaboration, communication, innovation and success. It is the policy of Philips to provide equal employment and advancement opportunities to all qualified employees and applicants for employment without regard to race, color, religion, sex, pregnancy/childbirth or related medical conditions, age, ethnic or national origin, sexual orientation, gender identity or expression, physical or mental disability, genetic information, citizenship status, veteran or military status, marital or domestic partner status or any other characteristic protected by law. As an equal opportunity employer, Philips is committed to fostering a culture where all are treated with respect and professionalism. To ensure reasonable accommodations for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans' Readjustment Act of 1974 and Title I of the Americans with Disabilities Act of 1990, applicants that require accommodation in the job application process may contact 888-367-7223, option 5, for assistance. Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace. Know Your Rights

Responsibilities

As a Process Quality Engineer, you will ensure that Philips products meet quality, safety, and regulatory standards while supporting QC activities and troubleshooting manufacturing abnormalities. You will also contribute to validation protocols and maintain documentation excellence.