Electronic Data Maintenance and Transfer Specialist
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 and Information Technology organisation, based in Netherlands.
• Transfer to suppliers: Exchange data with suppliers
• Communication person between company and supplier about DMR issues.
• Consulting on applicable standards, tools and assembly processes
• Manage lifecycle of components
• Improvement proposals: Learning from current way of working propose improvements
• Support: General support to development groups in the region regarding TPD and technical issues
• Expertise in CAD-E and CAD-M tools for data integrity purposes.
• Knowledge of FDA and IEC Standards
• Knowledge of Agile Sap and Windchill
• Be expert user in data storage and (meta-) data transfer tools, e.g. Agile, Windchill SAP-PLM, SAP-IPPe, PDX, ODB++ etc.
• Be expert user in version control of TPD, CAD-E and non-volatile PL data.
• Transfer of data on PCBA’s and assemblies to and from relevant suppliers, including Engineering Change and End-of-Life issues
• Obsolescence and EoL (End-of-Life) of electronic components.
• Guard process and procedure compliance in the data transfer process, e.g. reviews.
• Contribute in related process improvement activities.
• Work according to planning
• Work according to MR Quality Manual and MR Dev Q-Manual - especially regarding TPD, archiving and ECR (change control) procedures.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jurgen van Bergen.
The Company
The company is a large multinational in the medical devices industry.Role Description
As the Electronic Data Maintenance and Transfer Specialist, you are responsible to manage the lifecycle of electronic (including related mechanical) hardware data (integrity, status, transfer, obsolescence). You will work with a team of electrical, mechanical engineers, and manufacturing engineers to ensure that Technical Product Data (TPD), used for describing and creating hardware is transferred to suppliers and sub-contractors.Responsibilities
• Check integrity of CAD-E and associated assemblies and CAD-M data• Transfer to suppliers: Exchange data with suppliers
• Communication person between company and supplier about DMR issues.
• Consulting on applicable standards, tools and assembly processes
• Manage lifecycle of components
• Improvement proposals: Learning from current way of working propose improvements
• Support: General support to development groups in the region regarding TPD and technical issues
Requirements
• Someone with a master or bachelor (HBO) Degree in electronic engineering.• Expertise in CAD-E and CAD-M tools for data integrity purposes.
• Knowledge of FDA and IEC Standards
• Knowledge of Agile Sap and Windchill
• Be expert user in data storage and (meta-) data transfer tools, e.g. Agile, Windchill SAP-PLM, SAP-IPPe, PDX, ODB++ etc.
• Be expert user in version control of TPD, CAD-E and non-volatile PL data.
• Transfer of data on PCBA’s and assemblies to and from relevant suppliers, including Engineering Change and End-of-Life issues
• Obsolescence and EoL (End-of-Life) of electronic components.
• Guard process and procedure compliance in the data transfer process, e.g. reviews.
• Contribute in related process improvement activities.
• Work according to planning
• Work according to MR Quality Manual and MR Dev Q-Manual - especially regarding TPD, archiving and ECR (change control) procedures.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jurgen van Bergen.
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