Senior Software Advanced Quality Engineer - AI (Remote)

Work Flexibility: Remote or Hybrid or Onsite Senior Software Advanced Quality Engineer – AI (Remote) Stryker is hiring a Senior Software Advanced Quality Engineer, in Menlo Park, California supporting our DRE (Digital, Robotics, and Enabling Technology) business. As a valued member of Stryker’s AI innovation unit, you will work alongside trailblazers, industry visionaries, innovators, and inventors who are committed to bringing computer vision, AI/ML and digital innovation to the operating room and other healthcare settings. You’ll contribute to fast-paced cycles of innovation and develop core technologies that power a wide array of Stryker’s solutions, including: surgical robotics and navigation, image-guided surgery, treatment selection, outcome assessment, and clinical decision intelligence. You will apply your core skills across a range of deployment platforms spanning from mobile applications, cloud services, and SDKs to embedded systems, edge devices, and mixed reality (XR) platforms. You will have an opportunity to work across a wide variety of therapeutic areas ranging from orthopedics and neurosurgery to emergency care and operating room safety and efficiency – plus many more. Who we want: Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues. Motivated product launchers. Engineers who bring strategic direction and drive for execution to ensure products are developed and launched with precision. Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices. Goal-oriented developers. Keeping the customer and requirements squarely in focus, people who deliver safe and robust solutions. What you will do: Guide New Product Development teams through our Quality Management System (QMS) and Software Development Lifecycle (SDLC) process to ensure software is developed in compliance to internal procedures as well as the requirements of the FDA, ISO, and other related regulatory bodies. Conduct evaluation of software engineering activities of medical device new product development including requirements, software risk analysis, and design, development, documentation, integration, verification, validation, and release activities to deliver medical devices that are safe, secure and effective. Support software and system risk analysis and support the creation of software risk analyses to ensure safe and reliable products are launched to Stryker’s high-quality standards. Review and evaluate project tangibles for compliance as well as sound technical competence to ensure we are delivering robust products. Provide clear and timely feedback to stakeholders. Provide support to cross functional teams to ensure software quality objectives are met for medical device software development. Support critical analysis of technical situations and identification of problems. Work with cross-functional team in resolving the problems. Collaborate within cross-functional teams across multiple geographies to convey challenges, opportunities, solutions, and results in medical device new product development activities. Provide quality engineering input to impact the design, coding, and debugging of software in various coding languages including SOUP software. Support software build, maintenance, defect management, and change control activities. Collaborate with other engineering disciplines, such as electrical, mechanical, and industrial design, to ensure that software will accomplish design goals for a product or system. Support validation of new tools and approaches. What you need: Required BS in a science, engineering, or related discipline. 2 years of experience in the software engineering or quality field supporting new product development. Preferred Experience in medical device new product development preferred. Relevant work experience in software quality management of Class 2 or Class 3 medical devices including Software in Medical Device (SiMD) or Software as Medical Device (SaMD) preferred. Experience in interpreting industry standards for medical device development and updating processes and procedures preferred. Experience with and /or knowledge of the following desired: Quality Management System ISO 13485 SiMD IEC 62304 SaMD IEC 82304 FDA 21 CFR 820.30 FDA CFR Part 11 Compliance Knowledge of and experience with FDA General Principles of Software Validation IEC 14971 Risk Management IEC 81001-5-1 Health Software and Health IT Systems Safety, Effectiveness, and Security UL 2900-1 Cybersecurity Standard for Medical Devices Able to handle multiple tasks/projects and manage priorities accordingly. Technical writing ability - clear and concise writing easily understood by multiple audiences (auditors, peers, etc.). $83,000 - $176,800 salary plus bonus eligible benefits. Actual minimum and maximum may vary based on location. Individual pay is based on skills, experience, and other relevant factors. Travel Percentage: 10% Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World’s Best Workplaces! For more information, visit: www.stryker.com Work Flexibility Remote – Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location. Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based. Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category. Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.

Salary : $83,000 - $176,800