R&D Systems Intern
About The Position
The R&D Systems Intern will play a meaningful role in supporting both daily operational tasks and longer‑term projects that strengthen Sarepta’s R&D technology ecosystem. This internship provides hands‑on exposure to system analysis, troubleshooting, integrations, validation activities, documentation best practices, and project coordination in a regulated (GxP) environment. Beyond technical experience, this role also offers a unique opportunity for professional development, allowing the intern to explore leadership skills, deepen their understanding of the Life Sciences, and gain insight into the Biotech/Pharma industry. Through real project work and guided mentorship, the intern will be able to assess and potentially cultivate a future career interest in R&D Systems and drug development technologies.
Requirements
- Currently pursuing a Bachelor’s degree in Life Sciences, Information Systems, Computer Science, Data Management, Engineering, or related fields.
- Candidates who have successfully completed their second or third year of college would be strongly preferred.
- Curiosity about how digital systems support drug development in a GxP environment.
- Strong analytical, organizational, and problem ‑ solving skills.
- Ability to communicate clearly and work collaboratively with technical and non ‑ technical stakeholders.
- Attention to detail and willingness to learn structured documentation practices.
Nice To Haves
- Interest in AI applications and emerging technologies is beneficial but not .
Responsibilities
- Conduct systems analysis in support of various R&D systems–related projects.
- Troubleshoot issues and collaborate with business systems users to resolve problems efficiently.
- Assist with systems integration efforts across R&D platforms.
- Support and maintain Veeva Vaults under manager guidance.
- Develop, organize, and maintain spreadsheets and data trackers as needed.
- Participate in test script creation and execution for system validation.
- Gain exposure to a wide range of validation documents, including—but not limited to—URS, FRS, Validation Plans, PQ Protocols, Test Scripts, Traceability Matrix (TM), and Validation Summary Reports.
- Track the status of validated documents for assigned projects and follow up with cross ‑ functional teams before and after UAT/PQ activities.
- Learn and apply best documentation practices relevant to R&D Systems in a GxP / drug development environment.
- Assist with project management tasks and gain exposure to change management processes for validated systems.
- Explore the use of AI tools and technologies to improve R&D Systems support efficiency and change management workflows.
- Perform additional duties and project work as assigned.
Benefits
- Sarepta Therapeutics offers a competitive compensation and benefit package.
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What This Job Offers
Career Level
Intern
