Global Systems Integration Engineer
Organizational Area: Molecular
Country / State: Italy
Place of work: Bresso (MI)
Home / Office based: Office based
Reporting To: Global SD&I System Integration Manager
Job Scope
The Global Systems Integration Engineer is responsible for executing activities through out 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
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.
Education
Master’s Degree in Molecular Medicine.
Specialization/PhD: Appreciated but not required
Experience
Minimum of 3 years in a systems engineering, systems integration, or product development role.
Demonstrative 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.
Skills
- Highly motivated and success driven
- Understanding of system level product development
- Ability to understand interfaces between components in a complex product
- Ability to present complex problems through highest quality PPT presentations and effectively lead to proper decision making
- Scientific background in molecular field is an advantage
- Ability to escalate issues appropriately
- Strong analytical problem solving and decision making skills
- Good organizational and interpersonal skills
Languages
- English: fluent or mother language, both written and spoken
- Italian: fluent or mother language, both written and spoken
Seniority level
Associate
Employment type
Contract
Job function
Other
Industries
Medical Equipment Manufacturing and Pharmaceutical Manufacturing