Manufacturing Engineer (PR-34175760)

Manufacturing Engineer - Health Tech

As a Manufacturing Engineer you are responsible for define, improve and maintain the production processes within health-care.

You are responsible for

• Writing work instructions, monitor/maintain devices and tooling, instruct employees, implement and maintain production processes.
• Defect On Arrival (DEFOA) /Missing On Arrival (MOA) Root cause analysis, creating and implementing structural solutions.
• Providing structural solutions by initiating amendments like problem reports (PR) and/or 8D forms (Problem Solving methodology)
• Minimum disturbances (max.Yield) within production in cooperation with team leads, troubleshooters and development.
• Preparation and introduction of product changes through Life Cycle Management and New Product Introductions within the manufacturing process
• Participates as an expert in audits
• Give support and execute New Product Introductions.
• Support & execute Process Validation
• Providing input for the Manufacturing Engineer, to create a better way of working. After release for volume production the Sustaining Engineer is accountable for improvements.
• Analysis of performance data with respect to products and processes (Six-sigma, Statistical Process Control)
• Give input and maintain the New Product Introductions project planning.
• Perform preparation activities on trial/prototype production within New Product Introduction processes
• Defines and leads improvement projects for the assigned unit, to improve efficiency, product quality and test section (Green Belt).
• Investigation and escalation of Production issues/complaints, if needed together with development

To succeed in this role, you'll need a customer-first attitude and the following

• Typical bachelor in electronics or mechatronics or comparable. Master level is over-qualification.
• Hands-on mentality, proficient in documentation and natural inclination for accuracy.
• Be independent, pro-active, and not afraid to take ownership, including relevant stakeholders' management.
• A result & quality driven approach.
• Experience within Manufacturing or Engineering within high tech industry.
• Basic experience with OT (Operational Technology) and IT (Information Technology).
• Comprehension skills and ability to analyze and summarize.
• Technical knowledge to identify tooling issues and translate R&D requirements towards a manufacturing process, in collaboration with R&D and tooling suppliers.
• Experience with quality management and quality systems. Preferably experience in the medical industry (ISO 9001, 13485, FDA requirements, audits, FMEA, 8D, SPC, etc.).
• Personal & communication skills (Dutch & English)
• Communication with operators up to developers & management.

This role requires primarily a full-time attendance at the office, given the responsibilities in many situations cannot be carried out from home.

Please feel free to reach out in case of questions, and to have more information regarding the role.