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Company

Original Job Post

Abbott · 2 days ago

Senior Embedded Software Engineer

Pleasanton, CA

Full-time

Onsite

Senior Level

$96K/yr - $191K/yr

5+ years exp

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BiotechnologyEmergency Medicine

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Responsibilities

Perform software unit requirement analysis.

Prepare software unit architecture and designs.

Implement software units, perform peer code review, and create software unit tests.

Detect, report, investigate, disposition, and fix product defects.

Assist with escalated customer complaints investigations.

Perform timely, detailed CAPA engineering tasks.

Work with cross-functional teams – Quality, regulatory, EE, Systems, and Clinical teams.

Follow established guidelines for and participate in the review of product engineering artifacts.

Assist in the preparation and review of product and software development plans and reports as required.

Participate in the review and update of system specifications, designs, test descriptions, risk analysis, verification test procedures, and related documentation.

Travel approximately 5-10%.

Qualification

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C/C++Embedded SoftwareGUI DesignQt/QMLQt WidgetsLinuxRTOSMCU DevelopmentWi-FiNFCBLETest Case DevelopmentGTest FrameworkCeedlingSDLCJIRABitbucketConfluenceDOORSCMakeRisk ManagementSW FMEAIEC 62304Regulatory RequirementsMedical Device Industry KnowledgeDocumentation PracticesProblem-SolvingCollaborationCommunicationSoftware Engineering

Required

Bachelor’s degree in software engineering, Computer Science, Electrical Engineering or a related discipline.

5+ years of overall experience in software product development and 2+ years in the medical device industry.

C/C++ language embedded software experience.

GUI design and development experience with Qt/QML and Qt Widgets.

Operating systems like Linux or RTOS.

Experience with hardware, MCU development kits, and electrical test equipment.

Experience with Wi-Fi, Cellular, NFC and BLE.

Experience with selecting the best MCU for a product.

Experience developing test cases in C++ GTest framework or similar frameworks.

Experience developing test cases in C Ceedling or similar frameworks.

Understanding and appreciation of SDLC process and tools (e.g. JIRA, Bitbucket, Confluence, DOORS, CMake.)

Experience performing risk management analysis of software (e.g. SW FMEA techniques).

Knowledge within the medical device industry including IEC 62304 quality requirements and regulatory requirements or similar regulated experience.

Proven collaboration with cross-functional/multi-disciplinary teams.

Familiar with good documentation practices (software Design, data analysis, and reports)

Excellent verbal, written, and interpersonal communication skills

Preferred

Advanced degree in software engineering, Computer Science, Electrical Engineering or a related discipline, or related discipline with 2+ years of work experience in the medical device industry.

Experience with static code analysis tools such as Coverity.

Experience working in an Agile development environment.

Experience with Agile development methodologies.

Experience with Class II or III implantable medical device software development.

Strong knowledge of FDA and international regulatory requirements for medical device software