Key Responsibilities and Accountabilities:
* Define and develop system-level test tools to verify product safety and performance.
* Plan, execute, and document development, verification, and validation tasks within research and development projects.
* Analyze data using scientific tools (e.g., spreadsheets, graphical, statistical).
* Participate in research and development processes and meetings.
* Provide information to other teams regarding system needs and outputs, including presentations and meetings.
* Interact with external suppliers or partners.
* Supervise relevant activities conducted by other parties (technicians, suppliers).
Specific Responsibilities:
* Contribute to CE and FDA 510(k) submission testing activities.
* Improve the system.
* Supervise external contractors for testing activities (shelf-life, transport, biocompatibility, packaging integrity).
* Supervise production testing activities.
Knowledge, Skills, and Abilities:
* Solid understanding of physical systems, notably mechanical, fluidic, and sensor systems.
* Proficiency with statistical tools (e.g., regressions, model fitting, descriptive statistics).
* Programming skills: ability to develop and use scripts for data acquisition and analysis (a plus).
* Technical English writing skills: ability to write reports following QMS and incorporate results analysis concisely.
* Good communication skills within and outside the company, including with suppliers, contractors, and partners.
* Autonomous, team player, responsible, rigorous, and attentive to details.
Education and Experience:
* Engineering or equivalent university degree.
* Experience with medical device regulations is a plus.
Start of the Mission:
As soon as possible.
Application Process:
Please send your cover letter along with your resume.
Note: Only candidates with a Swiss passport or from UE-27 / AELE living in Switzerland with a B permit will be considered due to work permit processing times.
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