21 Mar

Software Engineer - Hyderabad - Medtronic

Position
Software Engineer
Company
Medtronic
Location
Hyderabad AP
Opening
21 Mar, 2017 7 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.

SUMMARY OF POSITION

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.

ESSENTIAL DUTIES AND RESPONSIBILITIES

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.

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

EXPERIENCE

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.

BASIC QUALIFICATIONS:
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

KNOWLEDGE, SKILL, AND ABILITY

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)

ORGANIZATIONAL RELATIONSHIPS/SCOPE:
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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