Intern – Systems Engineering (Sustaining & Design Controls) - San Diego, CA - Summer 2027

Start free →

Or apply yourself on the official page →

About the role

Job Title Intern – Systems Engineering (Sustaining & Design Controls) - San Diego, CA - Summer 2027 Job Description Are you interested in an Intern opportunity with Philips? We welcome individuals who are currently pursuing an undergraduate (BS) and/or graduate (MS) degree to participate in 3- 6 month paid Systems Engineering Intern opportunities at our site in San Diego, CA. Through this role you will gain meaningful, hands-on experience in medical device systems engineering, design controls, requirements management, risk management, and regulatory compliance within a leading HealthTech company.   You will work alongside experienced engineers to support the cutting-edge product portfolio by strengthening requirements traceability, risk management documentation, verification evidence, and technical documentation that demonstrate our products remain safe, effective, and compliant throughout their lifecycle.   Your role: • Work in a fast-paced R&D environment focused on developing innovative healthcare solutions. Support the maintenance and remediation of design control documentation, including requirements, verification records, risk management documentation, and technical file content. • Maintain end-to-end traceability between user needs, system requirements, design outputs, verification activities, validation evidence, and risk controls. Assist with impact assessments and regression analyses for product changes, identifying affected requirements, tests, risks, labeling, and documentation. • Support the development, review, and maintenance of Design Failure Mode and Effects Analyses (dFMEAs) and other risk management deliverables. Evaluate engineering requirements and verification records for clarity, completeness, consistency, and testability. • Collaborate with Systems Engineering, Quality & Regulatory, Verification & Validation, Human Factors, Software, Hardware, and project teams to resolve documentation and traceability issues. Assist in the preparation of technical documentation required for regulatory compliance activities, including EU MDR requirements. • Collect, organize, and review objective evidence to support regulatory submissions, technical documentation, and audit readiness activities. Support continuous improvement initiatives focused on engineering processes, documentation quality, and design control effectiveness, and present project progress, technical findings, and recommendations to engineering teams and management.   You’re the right fit if: • You are currently pursuing a Bachelor's or Master's degree in Systems Engineering, Biomedical Engineering, Electrical Engineering, Mechanical Engineering, Software Engineering or a related engineering discipline. • You have completed at least three years of undergraduate coursework or are currently enrolled in a graduate program. • You possess strong analytical skills and attention to detail when reviewing complex technical information. • You have foundational knowledge of systems engineering, requirements engineering, verification and validation, or risk management through coursework, projects, or internships. • You are interested in regulated medical device development and healthcare technologies. • You have strong problem-solving, troubleshooting, and root cause analysis skills. • You are proficient with Microsoft Office tools including Excel, Word, PowerPoint, and Visio. • You communicate effectively and work well both independently and within cross-functional teams. • You can establish and maintain productive working relationships with team members, stakeholders, and business partners. • You are a self-motivated learner with a desire to develop expertise in systems engineering and medical device product development. • You must be able to successf

View the official posting →