Why Sarepta? Why Now?
The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne.
We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.
What Sarepta Offers
At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity.
The Importance of the Role
The Opportunity to Make a Difference
Systems analysis in support of various projects associated with R&D systems
Troubleshooting issues and working with business systems users to resolve those issues
Assisting with systems integration
Support and maintenance of Veeva Vaults under manager's guidance
Spreadsheet development and organization, as needed
Participation in test scripts creation and execution
Gaining exposure to various validation documents, including, and not limited to, URS, FRS, Validation Plans, PQ Protocols, Test scripts, Traceability Matrix (TM), Validation Summary Reports, etc.
Under manager's guidance, keeping track of the status of validated documents associated with a project and following up with the business and other stakeholders before and after UAT/PQ execution
Learning and assisting with best documentation practices, as related to R&D Systems documents in the drug development field
Assisting with project management and gaining exposure with the change management process in a validated/GXP environment
Entertaining the use of AI and its application to making our R&D Systems support and change management process more efficient
Performing other duties, as assigned
More about You
The candidate will be majoring in a technical field (e.g., Engineering, Computer Science, or other related fields) and have, at least, successfully completed his/her freshman year from an accredited college/university. Candidates who have successfully completed their second or third year of college would be strongly preferred.
Interest in a career in the life sciences and drug development industry
Ability to work under manager's guidance and take ownership for assigned initiatives
Problem-solving skills
Program Timeline:
This application is for a 12-week summer internship program that will start on May 19th and conclude on August 8th, 2025.
What Now?
We're always looking for solution-oriented, critical thinkers.
So, if you're comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply.