In this role, you have the opportunity to
As a Sustaining Engineer you are responsible for giving support, improve and maintain the production process within the Sustaining Engineering Department Factory Best. Your primary focus will be data-analysis. You are also responsible for writing and maintaining work instructions for manufacturing processes.
You are responsible for
o Give support to Manufacturing New Product Introductions.
o Providing input for the Manufacturing Engineer, to create a better way of working, after RFVD the Sustaining Engineer is accountable for improvements.
o Analysis of performance data with respect to products and processes (Six-sigma, SPC)
o Give input and maintain the NPI project planning.
o DEFOA/MOA Root cause analysis, creating and implementing structural solutions.
o Perform preparation activities on trial/prototype production within NPI-processes
o Writing work instructions, monitor/maintain devices and tooling, instruct employees, implement and maintain production processes.
o Defines and leads improvement projects for the assigned unit, to improve efficiency, product quality and test section (Green Belt).
o Investigation and escalation of Production issues/complaints,.if needed together with development.
o Providing structural solutions by initiating amendments like problem reports (PR) and/or 8D forms
o Minimum disturbances (max.Yield) within production in cooperation with teamleads, troubleshooters and development.
o Preparation and introduction of product changes through Life Cycle Management/Business within production / systems.
You are part of
Factory Best, one of the largest Operations sites in Health Systems. Your part of Sustaining Engineering, a team which is responsible for processes within IGT/MR/SP&R/IC/RS. You will be working closely with the manufacturing and development department.
To succeed in this role, you should have the following skills and experience
o Typical bachelor in electronics or mechatronics.
o Experience with project management, quality management and quality systems. Preferably experience in the medical industry (ISO 9001, 13485, FDA requirements, audit planning and execution, FMEA, 8D, etc.).
o Experience within Manufacturing or Engineering with high tech medical devices.
o Preferably Green Belt or Lean certified.
o Six sigma / SPC.
o Comprehension skills and ability to analyse and summarise.
o A result driven and quality driven approach.
o Personal & communication skills (Dutch & English).