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Software Engineer II

4.00 to 6.00 Years   Hyderabad   17 May, 2023
Job LocationHyderabad
EducationNot Mentioned
SalaryNot Disclosed
IndustryMedical / Healthcare
Functional AreaGeneral / Other Software
EmploymentTypeFull-time

Job Description

    A Day in the Life Work with global R&D teams to develop software for new and existing medical device products. Software design and development of embedded real-time systems, including the development of Software Unit Test & Integration plans and protocols. Participates in reviews, code inspections and will support the development of documentation required for FDA device approval. Work effectively within a geographically dispersed and cross-functional teams during all phases of the product development process. Develop test automation framework and test scripts. Must be responsive, flexible, self-motivated and able to succeed within an open collaborative peer environment Is highly effective, agile and thrives in a dynamic environment with multiple, changing priorities Is comfortable with proactive outward communication and never shies away from a challenge Be Agile and effectively navigate through changing project priorities. Mentor, guide and train other engineersMinimum Qualification A Bachelor s degree in Computer science, Electrical, Electronics / equivalent from reputed institution. 4 to 6 years experience in Embedded Software development with at least four (4) years experience in the Medical device/Medical IT or regulated industry. Expertise in modern C++ (C++ 11 and above) software design & coding required in an Embedded development environment. Expertise of Object-Oriented Analysis & Design (OOAD) and familiarity with UML is strongly desired. Know-how in field-bus technology (EtherCAT preferred) and standard embedded communication protocols (DDS, SPI, I2C, AXI, UART, etc.) Desired experience with RTOS like Linux/WinCE/ThreadX etc with multi-threading, IPC knowledge. Experience working in a structured software development environment following a well-defined software development process like Agile / Lean. Experience with software risk analysis (per ISO 14971) including software failure mode and effects analysis (FMEA). Strong analytical skills and ability to multi-task. Superior written and verbal communication skills required. Strong interpersonal, presentation, and organizational skills. Awareness of Medical Device standards IEC 60601-1, IEC 62304, ISO 13485, ISO 14971 and applicable FDA standardsAdditional Information
    • Posting Date: Apr 27, 2023
    • Travel: Yes,
    ,

Keyskills :
environmentautomationprogrammingstorageanalyticssoftware design

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