Your key responsibilites are ?
Design and develop test processes, software and fixtures for new and sustaining products. Verify and validate test process and test fixtures to ensure targeted test coverage and effectiveness are met. Perform failure analysis, integration of test system modifications and certification of test process and fixtures. Maintain, create, and update manufacturing documentation as required.
Work with Product Development in Chatsworth and Marburg to ensure all products, subassemblies and modules meets manufacturability and test coverage requirements. Develop and implement manufactur-ability and testability requirements for new and existing products. Help transition test process, soft/firmware and test fixtures from R&D to production.
Design and develop test processes, software and fixtures for new and sustaining products. Verify and validate test process and test fixtures to meet targeted test coverage and effectiveness.
Develop and implement statistical process control methodology for new and sustaining products. Collect and analyze test data to identify problems, optimize processes and drive continuous process improvements including feedback to suppliers, manufacturing and R&D department. Establish test procedure for existing and new machines.
Actively participate in new product development by enforcing test and manufacturability design requirements, giving direct feedback in design reviews, reviewing and approving ECOs. Work close with outside supports teams for validation and calibration (e.g. Pharmaserv). Perform FMEA on manufacturing issues and implement improvements. Implement company policies and processes. Improve and refine processes to improve product quality. Perform all other duties as assigned.
Educational background and required skills:
B.S. in chemical or process engineering; 10 years in test process, program and systems development and resolving complex problems in chemical/medical manufacturing.
Must have experience in chemical and/or mechanical engineering from medical/pharmaceutical industry.
Extensive knowledge in control systems. Experience in coating and lamination with films, foils or papers. Ability to use MS Office, including spread-sheet and database programs, logic timing analysis equipment and statistical analysis. Good verbal and written communication skills, able to clearly explain results and their analysis, in both written and verbal reports.
Please apply with your CV and cover letter by the 'apply' button below
Remember - you found this opportunity on Qreer.com
| Education Backgrounds: |
Chemical Engineering |
| Specialties: |
Biomedical Engineering Biomedical Imaging / Modelling Process Engineering Process Management |
| Education Level: |
Undergraduate (Bachelors) Postgraduate (Masters) Doctorate (PH.D) |
| Experience: |
10 - 15 years 5 - 10 Years > 15 years |
| Languages spoken: |
English German |
| Job Location: | Krefeld, Germany |
Type: Job
Deadline: 9th May 2016
Job reference (ID): 8959
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