Job Details

• Design and implement complex software components and subsystems including object-oriented analysis and design, drafting design documentation and planning and conducting integrations and component tests.
• Support the design of the architectural concepts and basic framework of the product.
• Develop expert knowledge within the team of regulatory standards applicable to medical device and software development life cycle: ISO 13485, ISO 14971, and IEC 62304.
• Ensure a smooth transition from the product’s concept phase to maturity phase.
• Provide technical solutions to complex problems.
• Follow the company’s quality process and complies with quality management system procedures.
• Participate in software planning and estimating activities.
• Attends and supports engineering and surgeon review labs.
• Mentor/guide junior members of the team

• Highly skilled in C++, OOPS, Object oriented design and analysis, Multi-threading (POSIX).
• Expert level knowledge in Algorithms and data structures.
• Minimum 4+ years of experience in design and development.
• At least 2+ years’ experience in crating GUI applications using Qt, QML/QtQuick.
• Very good exposure of using QT Creator IDE
• Good knowledge of verification methodologies; Use of software developments tools, such as compilers, interpreters, programming editors, debuggers, source code control, defect management.
• Good exposure in Test Processes and Software Testing methodologies.
• Exposure to development of image processing applications.
• Demonstrated knowledge of regulatory standards and quality processes.
• Demonstrated communication and documentation skills.
• Must be able and flexible to work well under changing priorities in a high energy and demanding environment.
• Strong communication, analytical & problem-solving skills.
• Goal oriented with strong sense of responsibility and team player.

Reference ID - GH/Technology/JC//05122019//88093/SSE & Staff Engineer – Qt/QML/QtQuick