Career Opportunities: Staff Biomedical Engineer (62643)

Staff Biomedical EngineerWorking for Micro Systems Engineering, Inc. (MSEI) means joining an elite team to work on some of the most exciting challenges in medical technology today. We are a pioneer in developing innovative implantable medical device technologies and devices that save and enhance the quality of life for millions of individuals living with cardiovascular and chronic neurologic pain disorders. With more than 40 years of experience in design and manufacturing of active implantable medical devices, our continuing success is based on our company's core values - innovation, quality, reliability, integrity, teamwork, and undisputed expertise - thus enabling us to inspire confidence and trust in physicians and patients worldwide. We are continually looking for talented engineers, scientists, and professionals to share in our mission.Job Duties:Ensure that MSEI biomedical device design conforms to product specifications of extremely low power embedded real time applications.Develop test design documents and code.Generate and execute appropriate level of verification for each work product.Review test procedures generated by associate software verification engineers, as technical team lead.Review requirements specification and design and development work.Generate protocols, guidelines, and training sessions for the Software Verification team on proper verification test designs, as technical team lead.As technical team lead, work with internal contacts within a team, cross functional team contacts, as well as contacts with external vendors to discuss issues and lead scheduling coordination and task progress, with direction from management.Follow structured product development lifecycle in the medical device regulated environment.Serve as verification lead on projects and generate resource schedules, guidelines, protocols, and training sessions for the software verification team.Remain current in relevant software development processes, techniques, and tools.Remain current in the latest advances and developments in the application area for which the company generates products.Foster a culture of continuous process improvement.Approximately 10% of time will involve international or domestic travel per year. This is a hybrid position, requiring 2 days onsite in Lake Oswego per week.Requirements:A minimum of a bachelor's degree or the equivalent in Computer Science, Computer Engineering, or Electrical Engineering and 5 years of experience as a Software Engineer or Software Developer, or related position.5 years of experience performing software verification or software development.5 years of experience developing medical device software through writing code.5 years of experience working with Microsoft Visual Studio in a highly regulated environment developing automated tests with C#.5 years of experience utilizing the tools Git (Global Information Tracker) and Azure DevOps Source Control.5 years of experience with software lifecycle processes in a highly regulated environment (including FDA, ISO, and other regulatory bodies).2 years of experience performing software testing for the Bluetooth Low Energy (BLE) protocol.2 years of experience utilizing the HP (Hewlett Packard) Application Lifecycle Management tool.2 years of experience utilizing the Windows Power Shell scripting tool.1 year of experience administering Azure DevOps tools.1 year of experience utilizing the Aras (Software) Product Lifecycle Management tool.1 year of experience serving as technical lead in software project management (e.g., estimating efforts, creating project plans, tracking the project progress).Location: Lake Oswego, Oregon