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Job description
Job description
The System Verification & Validation group seeks an experienced Staff Engineer to support medical device new product development. This role focuses on developing software applications that automate verification and validation tests of implantable and external neuromodulation medical device software. The position also includes creating utilities that support automated verification, including integrations with third-party tool APIs and web-based tools. The successful candidate will contribute to test automation framework design using design patterns and sound object-oriented principles, while applying strong judgment to complex issues within established practices and policies.
PRIMARY JOB RESPONSIBILITIES
Participate in all phases of the Software Development Life Cycle process, including requirements definition, analysis and design
SW development with test frameworks and application to develop sophisticated automated tests for medical device software
Develop algorithms to solve complex problems - be able to understand and extend designs or come up with new design approaches
Contribute to test frameworks and tools, test design, documentation, test development/maintenance and test procedures used to drive automated test design and implementation
Review design documentation and code generated by other engineers - C#, C++
Execute tests to ensure conformance of code to requirements
Generate and maintain the appropriate work products
Review product design documents and test automation software
Other duties may be assigned at the discretion of the manager
Required profile
REQUIRED QUALIFICATIONS
BS or MS Degree in engineering in the field of Computer Science, Computer Engineering or Electrical Engineering or related field
6 years of graduate-level coursework and/or experience in software verification with considerable experience in creating and maintaining automated tests
Strong working knowledge of Microsoft Visual Studio development environment
Advanced knowledge of, and development experience with C#, C++ or Java
Experience working with configuration management, test management and defect tracking tools
Demonstrable success in driving one or more strategic projects to completion
2 years' experience in managing projects
PREFERRED QUALIFICATIONS
Experience with Test automation, Quality assurance experience desirable
Experience in mobile device application verification
Experience with software lifecycle processes in a medical device software (ISO 13485 & IEC 62304) or similarly regulated industry.
Experience creating automated test frameworks and test scripts for Kotlin-based software systems.
Ability to apply sound OO principles along with SW design patterns and practices
Ability to incorporate Claude Code into programming workflow for efficiency gains
TRAVEL REQUIREMENTS
Must be able to travel internationally and domestically, less than 5% of the time.
Company description
Micro Systems Engineering, Inc. (MSEI) is a pioneer in developing innovative implantable medical technologies that improve-and often save-the lives of millions living with cardiovascular conditions and chronic neurologic pain. With over 45 years of expertise in designing and manufacturing active implantable devices, our success is built on a foundation of core values: innovation, quality, reliability, integrity, teamwork, and deep technical excellence. These principles drive our global reputation for trust and confidence among physicians and patients alike. We're always seeking passionate engineers, scientists, technicians, and professionals to help advance our mission and shape the future of medical technology.
Please join us as:
Staff System Verification and Validation Engineer
What we offer
WORK ENVIRONMENT
If onsite, this role is based in a temperature controlled professional office setting, which may include an office or cubicle with quiet to moderate noise level. If remote, the work environment is the employee's residence. Work may need to be completed on campus in a lab, or manufacturing environment such as clean room or warehouse. Personal protective equipment is required in the clean room and may be needed in a lab. The noise level in the lab, and manufacturing environments are quiet to moderate. The role may travel to vendors, customers, external training, expos, industry or product events, and networking events shifting the work environment.
Worksite address
lake oswego, OR, 97034, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.