Sr. Software Quality Engineer - Medical Devices (Future Opportunity REF1459D)

Company Description

KMC Systems, an Elbit Systems of America company, offers an ecosystem of engineering and innovation to develop the most advanced clinical and operational solutions for leading medical device customers across a diverse range of market segments. KMC was established in Merrimack, NH, in 1980, conveying almost half a century of innovation, R&D of next generation devices, and the agility to evolve to meet changing market dynamics. This has kept KMC at the forefront of technological advancements and as the premier choice for leading global medical device and healthcare companies. KMC is a full-suite provider with services in: Engineering Design, Manufacturing, Product Ideation, Product Lifecycle Management, and Sustaining Engineering.

We are looking for extraordinary people to join #OneTeamOneMission to create and deliver innovative solutions that protect and save

We are currently recruiting for a future opportunity (Q4) for a highly talented Sr. Software Quality Engineer -- but we are looking for more than an impressive skill set.  We are looking for the type of person who respects others for their knowledge, skills, and experience as individuals and as team members. If you are the type of person who has high integrity and would thrive in an inclusive environment of camaraderie and friendship with your fellow teammates, we’re pretty confident you’ll love it here.

This position requires ONSITE work in our Merrimack, NH location - it is NOT a remote position.  We do offer a hybrid work environment.  

Job Description

1. Test software products for stability, usability, precision, accuracy, and reliability. Formulate and maintain test strategies; creating test plans and test cases for regression and functional testing of software products.

2. Work directly with the project team members, including software engineers, during key points along the software development process. Utilize the principals of the software development life cycle throughout the entire QA process.

3. Participate in product meetings throughout the development process to help guide the delivery of a quality product.

4. Utilize project planning and monitoring methods to ensure timely project completion.

5. Report problems via the defect tracking system Analyze, research, and track software defects through their resolution. Verify code fixes and sign off on resolutions.

6. Analyze test results and prepare SQA summary reports.

7. Establish and improve the SQA process/procedures.

8. Identify and recommend Software Quality Assurance testing tools and required equipment to develop software test suites, implement automated test cases with a focus on functionality, performance, code coverage and regression testing; report software problems, verify fixes and review user documentation.

9. Ensure that software used in the development and manufacturing of medical devices is in accordance with 13485, the QSR, and the KMC Quality Procedures.

10. Mentor less experienced members of the Software QA team.

Qualifications

• BS in Computer Science or related field with 5 or more years of related experience, or an equivalent combination of education and experience
• Able to work in a fast-paced, independent and team-based environment.  
• Must be detail-oriented individual with solid organizational, verbal and written communication skills.
• Able to communicate well with both technical and non-technical people.
• Knowledge of Risk Management and Risk Analysis process.
• Good understanding of QA processes and methodologies in a software development environment.
• Understanding of the Software Development Life Cycle.
• Experience with a version control system (i.e. CVS), Defect-tracking and automated testing tools.

Additional Information

·    US Citizens and those authorized to work in the USA without future sponsorship are encouraged to apply! 

All your information will be kept confidential according to EEO guidelines.

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