Process Quality Engineer

Philips Iberica SAU; Kepulauan Riau; On-site; IDR 200.000.000 - 300.000.000; Full time

Job summary

A leading health technology company in Indonesia is seeking a Process Quality Engineer to ensure stringent quality control of products. This role involves executing complex QC tasks, resolving manufacturing malfunctions, and maintaining compliance with regulatory standards. Candidates should have 4+ years of relevant experience and a degree in engineering or life sciences. The position demands attention to detail, strong analytical skills, and the ability to work independently. Join a team dedicated to improving healthcare quality worldwide.

Qualifications

• At least 4 years relevant experience in manufacturing quality or QC within a regulated environment.
• Strong understanding of GLP, GMP, and core regulatory expectations.

Responsibilities

• Execute diverse and complex quality control tasks using technical knowledge.
• Assist in resolving complex malfunctions and perform quality inspection activities.
• Implement quality control procedures to ensure adherence to GLP and GMP.

Skills

GLP

GMP

SPC (Statistical Process Control)

Minitab

Statistical analysis

CAPA processes

Problem-solving methodologies

Analytical thinking

Education

Bachelor’s degree in Engineering, Life Sciences, or related technical field

Job description

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.