Sustaining Engineer
Location: NetherlandsSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Medical Devices organisation, based in Noord-Brabant Netherlands.
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.
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).
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rowin van der Zwaan.
Role Description
As a Sustaining Engineer you are responsible for giving support, improve and maintain the production process within the Sustaining Engineering Department. Your primary focus will be data-analysis. You are also responsible for writing and maintaining work instructions for manufacturing processes.Responsibilities
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.
Requirements
o 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).
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rowin van der Zwaan.
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