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
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