Chaberton Professionals, a division of Chaberton Partner s dedicated to the research and selection of Middle Management profiles, is currently looking for a Global Systems Integration Engineer – Molecular for a medical device-diagnostics company.
Your Mission
The Global Systems Integration Engineer is responsible for executing activities throughout the product development lifecycle including:
* Feasibility testing and optimization
* Development activities, including system verification and validation
* Assay integration and validation
* Assessing and supporting system reliability
* Problem solving related to software, hardware, consumables, and assay integration
* Hands-on troubleshooting
* Requirements management and product definition
* Risk management
Main Responsibilities
Work on the development and integration of systems and subsystems designed for medical diagnostics, including: instruments, related equipment and fixtures, software, consumables, and assay protocol and chemistries.
Write System requirements/specifications
Review hardware and software requirements/specifications
Perform system feasibility, optimization, and V&V activities in line with other key functions in the Company.
Write and execute test protocols for system level testing
Assess system reliability, and support reliability testing activities
Present work and experimental result, to key stakeholders, through high quality PowerPoint presentations
Ensure the quality of technical documentation in compliance with all the Company's requirements including Quality Assurance requests
Work cross-functionally with other company functions (including R&D, Quality Assurance, Corporate Service, Business, and Operations) in driving successful product development and owning technical expertise on systems integration competencies
Work with 3rd party instrumentation suppliers on instrument development, as required by the project.
Requirements
Master’s Degree in Engineering or Sciences, preferably with emphasis on Biomedical Engineering.
Technical Competencies: Ddmonstrative technical proficiency, scientific creativity, collaboration and a successful track record that has involved independent thinking.
Preferably the candidate should have experience working in medical device industry, developing products that are subject to CE marking or FDA approval.
Italian and English: fluent or mother language, both written and spoken
Location : Milano