[ref. p19490722] Manufacturing Process Technologist

• Design and develop new manufacturing processes and systems to enhance efficiency, productivity and quality.
• Analyse and optimise existing processes to reduce waste, improve performance and maintain consistent product quality.
• Implement and maintain process control strategies that ensure smooth operations and compliance with quality standards.
• Collaborate across disciplines to integrate new technologies into existing or new systems with minimal disruption.
• Evaluate and recommend new equipment and technologies to keep manufacturing operations future-ready and competitive.

You'll work in cross-functional teams and make a direct impact on how cutting-edge medical equipment is made.

You can count on:

• A monthly salary between €4000 - €5300 depending on your experience.
• A flexible benefits package and the option to purchase additional holidays (26 standard days).
• Hybrid working possibilities - from home or at the office.
• A company pension scheme and access to a collective health insurance.
• Discounted gym memberships, cultural outings and wellness programmes.
• Extensive training and growth opportunities, including access to the Brunel Academy.

Over Brunel

You'll benefit from excellent employment conditions, personal coaching, and continuous learning.

You are a strong communicator and team player who thrives in an innovative, high-tech environment. You take initiative, solve problems effectively, and have a keen eye for continuous improvement. You're comfortable working internationally and enjoy collaborating across cultures and disciplines.

In addition, you have:

• A Master's or PhD degree (or equivalent) in Engineering.
• At least 5 years of experience in manufacturing process development or as a process technologist.
• Strong analytical skills with the ability to solve fundamental issues using deep technical knowledge.
• Proven experience in process optimisation and control strategies.
• Expertise in medical equipment or manufacturing systems.
• Knowledge of regulatory requirements for medical device development.
• Willingness to travel up to 25% and/or work at customer locations across Europe.