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 organisation, based in Noord-Brabant Netherlands.
- Providing input for the Manufacturing Engineer, to create a better way of working, after RFVD the Sustaining Engineer is accountable for improvements.
- Analysis of performance data with respect to products and processes (Six-sigma, SPC)
- Give input and maintain the NPI project planning.
- DEFOA/MOA Root cause analysis, creating and implementing structural solutions.
- Perform preparation activities on trial/prototype production within NPI-processes
- Writing work instructions, monitor/maintain devices and tooling, instruct employees, implement and maintain production 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.
- Providing structural solutions by initiating amendments like problem reports (PR) and/or 8D forms
- Minimum disturbances (max.Yield) within production in cooperation with teamleads, troubleshooters and development.
- Preparation and introduction of product changes through Life Cycle Management/Business within production / systems.
- 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.).
- Experience within Manufacturing or Engineering with high tech medical devices.
- Preferably Green Belt or Lean certified.
- Six sigma / SPC.
- Comprehension skills and ability to analyse and summarise.
- A result driven and quality driven approach.
- 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 Robin Hiariej.
Role Description
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.Responsibilities
- Give support to Manufacturing New Product Introductions.- Providing input for the Manufacturing Engineer, to create a better way of working, after RFVD the Sustaining Engineer is accountable for improvements.
- Analysis of performance data with respect to products and processes (Six-sigma, SPC)
- Give input and maintain the NPI project planning.
- DEFOA/MOA Root cause analysis, creating and implementing structural solutions.
- Perform preparation activities on trial/prototype production within NPI-processes
- Writing work instructions, monitor/maintain devices and tooling, instruct employees, implement and maintain production 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.
- Providing structural solutions by initiating amendments like problem reports (PR) and/or 8D forms
- Minimum disturbances (max.Yield) within production in cooperation with teamleads, troubleshooters and development.
- Preparation and introduction of product changes through Life Cycle Management/Business within production / systems.
Requirements
- Typical bachelor in electronics or mechatronics.- 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.).
- Experience within Manufacturing or Engineering with high tech medical devices.
- Preferably Green Belt or Lean certified.
- Six sigma / SPC.
- Comprehension skills and ability to analyse and summarise.
- A result driven and quality driven approach.
- 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 Robin Hiariej.
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