System Engineer

L&T Technology Services is looking for candidates in Bangalore location for the position of System Engineer.

Job description:

Experience: 7 to 12 years

Notice period: Immediate to 30 days

Location: Bengaluru

Mandate skills: Medical device experience, traceability matrix, system requirements, FMEA, Risk management, Risk analysis, Hazard analysis, knowledge on CAPA, DOORS tool(optional)

Experience in successfully developing complex medical device (hardware, software, consumables) products, Defines User Requirements, system requirements, FMEA, architecture, and interfaces to meet product requirements, risk analysis and industry standards; conducts system design analysis to select key components and defines control methods; and coordinates build and design integration, Experience with Sustenance Engineering, Change review Board, Defect Management, Knowledge of medical regulations and standards, Experience in MRI domain will be added advantage.

• MS or PhD in relevant field including Computer, Electrical, Mechanical Engineering, or other related science. 
• A minimum of 8 years of experience successfully developing complex medical device (hardware, software, consumables) products for acute care/hospital markets is necessary.
• A minimum of 6 years of hands-on experience (technical) in ventilation is necessary.
• Hands on experiences in Model Based Systems Engineering
• Experience with conducting cross-discipline feasibility and trade off studies to evaluate electronic, mechanical, and pneumatic performance from subsystem to system level for issue resolutions
• Analytical and architectural thinking, system view, physical insight, flexibility, and a hands-on mentality to deliver sustainable results and creative solutions.
• Strong understanding of Controls and Software development process including Model-based Design approach and Test-Driven design methodologies
• Solid understanding of System Verification and Validation test plan/protocols, executing V&V (Verification and Validation) (Verification and Validation) activities, generating, and analyzing test reports
• Understanding of global medical device regulatory environments and clearance processes.
• Effective communication, computer, documentation, presentation, and interpersonal skills are required, as well as the ability to work both independently and as part of a team.