Co-op – Software Design Assurance (IGTD) – Plymouth, MN – January 2027
About The Position
This co-op opportunity at Philips in Plymouth, MN is for individuals currently pursuing an undergraduate (BS) and/or graduate (MS) degree. The role offers paid internship and co-op experience within a HealthTech company. The co-op will support the Software Design Assurance team in various aspects of software-intensive medical device programs. This includes assisting with software lifecycle compliance, documentation reviews, requirements traceability, quality metrics, and audit-readiness. The co-op will collaborate with multiple departments such as Software Design Assurance, Software Development, Systems Engineering, Regulatory Affairs, Product Security, and Quality to support product development and process improvement. Specific tasks involve assisting with design and technical review preparation, risk management documentation, verification evidence, cybersecurity and Software Bill of Materials documentation, and organizing compliance records. The role also supports digitalization and continuous improvement efforts, including process mapping, dashboards, knowledge management, and the adoption of AI-based software lifecycle tools. The co-op will gain practical knowledge of medical device design controls, software lifecycle processes, risk management, cybersecurity, and quality systems within a hybrid office environment.
Requirements
- Pursuing a Bachelor’s or Master’s degree in Software Engineering, Computer Science, Biomedical Engineering, Computer Engineering, Systems Engineering, Electrical Engineering, or a related technical field.
- Strong analytical thinking, attention to detail, organization, and written and verbal communication skills.
- Must be able to successfully perform the minimum Physical, Cognitive and Environmental job requirements with or without accommodation.
Nice To Haves
- Familiarity with software development, testing, Agile methods, requirements management, data analysis, or cybersecurity is a plus.
- Experience gained through university projects, coursework, laboratories, prior internships, or co-ops is welcome.
- Exposure to Python, Power BI, SharePoint, Git, Azure DevOps, Codebeamer, or similar tools is a bonus.
Responsibilities
- Help the Software Design Assurance team support software-intensive medical device programs by assisting with software lifecycle compliance, documentation reviews, requirements traceability, quality metrics, and audit-readiness activities.
- Collaborate with Software Design Assurance, Software Development, Systems Engineering, Regulatory Affairs, Product Security, and Quality partners to support product development and process improvement initiatives.
- Assist with design and technical review preparation, risk management documentation, verification evidence, cybersecurity and Software Bill of Materials documentation, and organization of compliance records.
- Support digitalization and continuous-improvement work, including process mapping, dashboards, knowledge management, and adoption of AI-based software lifecycle tools and workflows.
- Build practical knowledge of medical device design controls, software lifecycle processes, risk management, cybersecurity, and quality systems while working in a hybrid office environment.
Benefits
- Paid internship and co-op opportunities
- Overtime eligible
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What This Job Offers
Job Type
Full-time
Career Level
Intern
Education Level
Associate degree
