Manufacturing Engineer IGT Process Validation

Job Title: Manufacturing Engineer IGT

Location: Best, Netherlands (Hybrid possible)

Department: Imaging Guided Therapy (IGT) Factory

Duration: 1 year with the possibility of extension

Job Type: Contract, Full-time

Drive process improvements and innovation in a high-tech medical manufacturing environment.

Your Role

As a Manufacturing Engineer, you will support, improve, and maintain production processes within the IGT Factory at Philips' Manufacturing Department in Best. Factory Best is one of the largest medical manufacturing sites within Health Systems. The Manufacturing Engineering team oversees processes in Imaging Guided Therapy (IGT), Magnetic Resonance Imaging (MR), Service, Parts & Repair (SP&R), Imaging Components (IC), Refurbishment Systems (RS), Digital X-Ray (DXR), and Parts Recovery (PR). You will collaborate closely with operations, quality, and development teams to ensure optimal production performance.

Your responsibilities include analyzing performance data related to products and processes using methodologies such as Six Sigma and Statistical Process Control (SPC), releasing and validating both new and existing processes, and providing structural solutions through amendments such as Problem Reports (PR) and 8D problem-solving methodologies. Additionally, you will act as a process validation expert during audits.

Key Responsibilities

• Analyze performance data using Six Sigma and Statistical Process Control methodologies

• Release and validate new and existing manufacturing processes

• Provide structural solutions through amendments such as Problem Reports (PR) and 8D methodologies

• Act as an expert in audits and support process validation

• Work closely with operations, quality, and development teams to optimize production performance

You're the Right Fit If You Have

• A bachelor’s or master’s degree in Biomedical Engineering, Applied Physics, or a comparable field

• Strong documentation skills and attention to detail

• An independent and proactive attitude with the ability to take ownership and manage stakeholders effectively

• A results- and quality-driven mindset

• Preferably experience in process validation or a background in quality

• At least two years of experience in manufacturing or engineering within the high-tech industry

• Strong analytical and summarization skills

• Experience with quality management systems, preferably in the medical industry (ISO 9001, ISO 13485, FDA requirements, audits, FMEA, 8D, SPC, etc.)

• Strong communication skills, with the ability to engage effectively with operators, developers, and management

What You’ll Gain

When you choose to work at Philips, you’ll contribute to life-changing projects and innovative healthcare solutions that impact lives worldwide. This opportunity will allow you to gain new experiences, develop new skills, and expand your professional network.

For Contract Roles

For this project, you will work for Philips as a contract or permanent employee of a Randstad company. As a contractor at Philips, you'll take on cutting-edge challenges that will enhance your expertise. As an employee of a Randstad company, you will receive various benefits, including ongoing support for personal development and career growth.

About Philips

Philips is a global leader in health technology, committed to improving lives through meaningful innovation. As a contractor or freelancer at Philips, you’ll be part of a diverse and collaborative team, contributing to solutions that make a real impact on healthcare worldwide. The Randstad companies are responsible for recruiting talent for Philips. If selected for this role, you will be employed by a Randstad company, not Philips directly.