Stryker is looking to ensure the quality and compliance of their software for the LIFEPAK 35 device by coordinating software testing throughout the development lifecycle.
Requirements
- 4+ years of product testing in a product development environment
- Advanced knowledge of software verification activities integrated within a software development cycle
- Experience owning product feature areas and ability to estimate work effort
- Advanced knowledge of software version control tools
- Experience with software test equipment and test methodologies
- Experience in a medical device or regulated product development environment (21 CFR 820 regulations and ISO 13485 medical device standards)
Responsibilities
- Develop and maintain integrated software verification activities with limited supervision
- Perform software verification activities including test creation, execution, debug, and resolution of issues
- Produce complete, concise, clear and technically correct work outputs
- Apply knowledge of a high level programming language to create new test protocols and debug existing test protocols with limited supervision
- Utilize the requirements management systems (JAMA) independently
- Create and track software defect records in the defect tracking database
- Drive initiatives to improve product testing and design assurance processes, including suggesting technical enhancements and evolving best practices and tools
Other
- This role is hybrid expecting at least 3 days a week in the Redmond, WA office
- 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/Veteran/Disability.
