21 Mar

Software Engineer - - Medtronic

Software Engineer
21 Mar, 2017 30+ days ago

Medtronic as the company that open the jobs vacancy, have some qualification and spesification especially for the Software Engineer jobs vacancy. To find out more information and about qualification and spesification details, walkin interview schedule, the address of the company, the company contact info (email/phone number) of Medtronic company, please start to apply for the job vacancy with fill the jobs application with click the 'Apply This Job' button below.


The Lead Engineer / Senior Software Verification and Validation Engineer will be responsible for various Software Verification and Validation during the development lifecycle of complex electro-mechanical medical devices.

The individual will be a part of a professional Software Verification and Validation team and will work closely with software development engineers and other cross functional teams

The overall job of the Senior Software Verification and Validation Engineer is one of contributing positively in creation and innovation, which would lead to the development and introduction of new and tailored products.

Work with minimum supervision, with interdisciplinary team of SVA engineers and technicians to execute test plans to support the Design Validation of CRHF systems and products. Contribute to test strategy, plans, test development, and lead test execution.


Execute Design validation protocols, interpret test results, and author test result reports.

Work closely with lead Validation engineer and Project design teams to ensure coverage between requirements & validation test protocols.

Contribute System Design Validation testing strategies, plans, and reports as needed to fulfill the Design Validation deliverables.

Take ownership of assigned test protocols with responsibility to independently identify, resolve if possible, and promptly communicate issues found in the test protocol, test equipment, test execution, or test results.

Build domain knowledge of CRHF product and systems, clinical environments of use, as well as existing test tools and methodologies. In particular, the creation of cardiac test data using simulated inputs.

Follow the CRHF QSR, and ensure personal understanding of all quality policy/system items that are personally applicable. Follow all work/quality procedures to ensure quality system compliance and high quality work.

Expected to balance a complex work load while delivering timely completion of testing activities. Manage assigned validation tasks, and communicate plan and status of tasks to SVA test request owners.

Identify, propose, and assist in the implementation of process improvement initiatives that significantly improve the operational effectiveness of the SVA organization and/or improve the efficiency and effectiveness of the Design Validation process.

Ability to overcome technical problems encountered that require understanding of broader Medtronic systems and how they interact.

Develop and document test fixtures, test methods and other test equipment, and maintain and calibrate test equipment.

Build capability to conduct field testing with Medtronic clinical partners.


Masters or Bachelors of Engineering Degree in Biomedical Engineering, Electrical Engineering, Software Engineering or related field.


Required: A minimum of 8 - 12 years in Software Verification & Validation.

Preferred: 8 years’ experience in software testing and quality assurance of which minimum 3 years’ experience should preferably be in the medical device field

Experience in Biomedical Engineering, Electrical Engineering, Software Engineering or related field.


Ability to work under limited supervision and follow general direction for work

Ability to perform the test development and execution relative to Design Verification and/or Design Validation, requiring considerable judgment in determining work methods, interpreting test results and writing clear and accurate test result reports.

Experience in Biomedical Engineering, Electrical Engineering, Software Engineering or related field.

Experience in requirement engineering and familiarity with requirement management tools.

Experience with Verification and Validation Testing Methodologies

Quality System Regulation experience relative to Design Verification and/or Design Validation.

Technical writing and communication

Ability to plan and estimate project tasks to support successful completion of Design validation

Ability to provide leadership to lower level personnel


Experience in planning and executing Design Validation

Familiarity with FDA Quality System Regulations (820.30 design controls), ISO 13485, and IEC62304 is preferred.

Engineering experience in a medical device field

Hands-on experience with remote monitoring and/or remote follow-up of cardiac patients.

8 to 10 years of experience in Software Verification and Validation.

Test experience with complex systems that include

Bluetooth communications

mobile OS based applications (Android, IOS)

cloud based software and embedded firmware

interfaces with multiple external SW systems (example: Electronic Health records, Data management systems)


Reports to the Software Manager for functional leadership.

Frequent interaction with Software Developers, team members from other disciplines to develop test requirements and other project artifacts. Possible interaction with third-party vendors, clinical partners.

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