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R&D Engineer, Combination products Contract (m,w,d) (EN)
[13500]
design control, risk management, Process Development, Human Factors
Job title: R&D Engineer, Combination products Contract (m,w,d) Industry: Pharma & Medizintechnik Skills: design control,risk management,Process Development,Human Factors Start of project: ASAP Duration of the project : 12 months Project volume: 1920 Hour(s) Location: Neuchatel, CH Tasks: ·Applies engineering principles with minimal guidance in the design and development of robust devices and drug/device combination products ·Able to independently tackle sophisticated problems using tools such as: engineering modelling and simulation tools, design and prototyping tools, statistical analysis, benchtop experiments and analysis, usability engineering tools, design for manufacturability/assembly techniques and design for six sigma. ·Solid understanding and experience with regulations and standards such as design controls, risk management, human factors and industry standards specific to an individual’s subject area Qualifications: ·Experience and detailed understanding of medical device development (ISO 13485) ·Proven experience of product characterization, design controls and risk management ·Extensive experience of working in a multi-functional product development environment ·Excellent interpersonal skills (both written and oral) to summarize development work, critical conclusions and its relevance to the bigger picture
Skills: design control,risk management,Process Development,Human Factors
- Applies engineering principles with minimal guidance in the design and development of robust devices and drug/device combination products
- Able to independently tackle sophisticated problems using tools such as: engineering modelling and simulation tools, design and prototyping tools, statistical analysis, benchtop experiments and analysis, usability engineering tools, design for manufacturability/assembly techniques and design for six sigma.
- Solid understanding and experience with regulations and standards such as design controls, risk management, human factors and industry standards specific to an individual’s subject area
- Experience and detailed understanding of medical device development (ISO 13485)
- Proven experience of product characterization, design controls and risk management
- Extensive experience of working in a multi-functional product development environment
- Excellent interpersonal skills (both written and oral) to summarize development work, critical conclusions and its relevance to the bigger picture
Gaziza Konuspayeva