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Process Development Technologist Eindhoven SIRE Life Sciences

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Gevraagd

  • 37 - 40 uur
  • Medior/Senior
  • Engels (taal)

Aanbod

  • Vast contract
 

Vacature in het kort

Eindhoven
Join a leading global health technology company as a Process Development Technologist and play a pivotal role in advancing the manufacturing of high-quality medical devices. Focus on enhancing efficiency, productivity, and product quality through innovative process design and technology integration. Collaborate with cross-functional teams and support international projects, with opportunities for occasional travel. Be part of a mission-driven environment committed to meaningful innovation in healthcare. Find out why this job might be the perfect match for your skills.
 

Over het bedrijf

SIRE Life Sciences
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The Company 
Our client is a leading global health technology company focused on improving people’s health and well-being through meaningful innovation. With a strong legacy in healthcare and consumer technology, Philips develops cutting-edge solutions in diagnostic imaging, patient monitoring, image-guided therapy, and health informatics.

The Role
As a Process Development Technologist you will play a key role in developing and optimizing manufacturing processes for high-quality medical devices. You’ll work on improving efficiency, productivity, and product quality by designing innovative process solutions, analyzing current systems, and integrating new technologies.

Responsibilities

  • Develop and design innovative manufacturing processes to improve efficiency, quality, and productivity.

  • Analyze and optimize existing manufacturing workflows to reduce waste and enhance performance.

  • Implement and maintain process control strategies to ensure consistent and reliable operations.

  • Collaborate with cross-functional teams to integrate new technologies into existing or new manufacturing systems.

  • Evaluate and recommend new equipment or technologies to improve manufacturing capabilities.

  • Ensure compliance with quality standards and medical device regulations during process development and deployment.

  • Support international projects, including occasional travel (up to 25%) for on-site implementation and collaboration.

Requirements
  • MSc or PhD in Engineering or a related technical discipline.
  • At least 5 years in manufacturing process development, with proven expertise in process optimization, control strategies, and working within medical equipment or manufacturing systems.
  • Solid understanding of medical device regulations and quality standards relevant to manufacturing environments.
  • Strong problem-solving, communication, and teamwork skills; GreenBelt or BlackBelt certification (or equivalent) is preferred.
  • Willingness to travel internationally up to 25% and work on-site with customers as required; this position is not open to freelancers or relocation.
 

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