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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Principal Systems/Verification Engineer (Aesthetic... - **Company:** Bausch Health - **Location:** Bothell, WA, United States - **Experience:** Expert - **Salary:** $115,000.0 - $158,000.0 - **Contract:** Permanent contract - **Skills:** C (Programming Language), .NET Framework, Adobe InDesign, Systems Engineering, JIRA, Automation of Tests, Bug Tracking Systems, C Sharp (Programming Language), C++ (Programming Language), Code Review, Linux on Embedded Systems, Issue Tracking Systems, MATLAB, Microsoft Project, Regression Analysis, Requirements Management, Software Requirements Analysis, Test Execution Engine, Microsoft Windows CE, Test Scripts, System-level Testing, Visual Basic Language - **Published:** July 23, 2026 - **Apply:** https://www.juju.com/job/00000000gkh13q ## About the Role * BS or MS in Engineering plus ten years of experience designing / validating / testing of complex electro-mechanical systems, and at least five years in medical devices or closely related field. * Knowledge / experience in System Engineering concepts/principles. * Experience with C# and .NET desired * Verification experience with embedded platforms including Windows CE and Embedded Linux desired * Proven track record of successful product testing, verification, and validation using a variety of testing tools and techniques. * Ability and willingness to support project planning and management including use of scheduling software such as MS Project. * Demonstrated experience on the use of a requirements management tool (e.g. DOORS/DOORS NG) for requirements trace management * Ability to focus on and achieve scheduled milestones, including contingency planning. * Ability to operate test equipment such as oscilloscope, logic analyzer, etc. * Competency in at least one of the following: C++, C#, Visual Basic, or Matlab. * Use of defect tracking tools such as TestTrack, JIRA, etc. * Knowledge of FDA Quality System and Design Control requirements and their application to projects from design inception to manufacturing release. * Regulatory experience in QSR, ISO13485. * Risk Management techniques and experience in EN 14971:, * Experience in Usability Engineering compliant to EN IEC 62366:. * Experience producing designs compliant to EN IEC 60601-1 /-2:, EN IEC 62304: Medical Device Directive Essential Requirements. Working experience with ESD environment. * Strong team collaboration and communication skills. * Driven to get the job done in the face of obstacles and time constraints, and a willingness to jump in wherever needed. * Demonstrated ability to multi-task. Language and Verbal Skills Ability to read, analyze, and interpret engineering specifications, general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to write reports, specifications, business correspondence, test plans / protocols and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public. Ability to clearly and concisely convey project accomplishments, obstacles, issues, and status to project team members. Math Skills Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry. Ability to use basic engineering tools to perform calculations and simulations and interpret project results/data. Analytical and Reading Skills Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. Ability to read technical and clinical literature and documents and extract important concepts. ## Description The Principal Systems/Verification Engineer confirms Solta products meet functional system requirements. The applicant must be a hands-on self-starter, who has the ability to work collaboratively with a multi-disciplinary product development team in support of all aspects of component and systems level verification testing of medical devices. This person will develop and manage component and system level testing consistent with product system requirements in accordance with the Company, applicable standards (e.g. IEC14971, IEC60601, & ISO13485), FDA and other requirements, identifying and developing test methods and individual test cases across multiple products; Principle Responsibilities and Duties: Note: The following is meant to be representative but not necessarily all inclusive of the duties and responsibilities for this position title. * Develop System/SW verification Tests using C, C++ and C# * Develop tests for device software, including automated tests. * Lead / participate in Design and Code reviews * Demonstrated experience with Medical Device System/SW verification for Windows CE based devices and Embedded Linux based devices. * Coordinate / conduct Design Verification testing (embedded Linux / C#) * Provide technical leadership / mentoring - especially in applicable test methods of products * Develop plans and coordinate activities for system level verification testing, including regression analysis of system functionality to determine scope of testing, overseeing test execution and reviewing individual test results and data for inclusion with test reports. * Write individual and summary level test reports which provide clear and concise results along with appropriate detail information as needed. * In partnership with other system engineers, formulate system functional requirement specifications and risk assessments. * Establish and maintain product requirements and verification trace management via a requirements management tool. * Identify test cases and write verification test protocols for software and hardware verification/validation that utilize manual and automated test methods. * Design and/or develop verification scripts to utilize automated test methods * Develop verification test scripts and protocols utilizing automated and manual test methods. * Address and analyze functionality and performance related issues discovered during verification testing. * Document results of work activities. * Participate in defect issue tracking, troubleshooting, and resolution. * Identify and isolate product defects, perform root cause analysis, and work with engineering team across design disciplines to determine corrective action. * Work closely with other departments to ensure projects conform to all regulatory and quality regulations., While performing the duties of this job, the employee may be required to perform lifting tasks of up to 10 pounds for short durations. The employee will be required to use a computer for up to 8 hours consecutively Duties of this job may involve standing and/or walking for extended periods of time. Duties also involve daily keyboard data entry. Specific vision abilities required by this job include close vision and color vision. Work Environment The noise level in the work environment is usually moderate. Some light machining and prototyping activities will involve moderate noise levels (i.e. power drill) and moderate dust or debris exposure. Safety Solta is committed to the health and safety of our employees. We expect that all employees will perform their responsibilities while maintaining a safe, cooperative, and productive work environment, thus ensuring the health and safety of themselves and others. ## Related Videos - [Are Code Reviews Worth It? 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