R&D Systems Intern

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profile Job Location:

Cambridge, MA - USA

profile Hourly Salary: $ 21 - 26
Posted on: 3 hours ago
Vacancies: 1 Vacancy

Job Summary

Why Sarepta Why Now

The promise of genetic medicine has arrived and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle central nervous system and cardiac 2023 we launched our fourth therapy and the first ever gene therapy to treat Duchenne.

Were 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 R&D Systems Intern will play a meaningful role in supporting both daily operational tasks and longerterm projects that strengthen Sareptas R&D technology ecosystem. This internship provides handson 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.

The Opportunity to Make a Difference

  • Conduct systems analysis in support of various R&D systemsrelated 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 includingbut not limited toURS 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 crossfunctional 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.

More about You

  • Currently pursuing a Bachelors 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 problemsolving skills.

  • Ability to communicate clearly and work collaboratively with technical and nontechnical stakeholders.

  • Attention to detail and willingness to learn structured documentation practices.

  • Interest in AI applications and emerging technologies is beneficial but not .

Program Timeline

This application is for a 12-week summer internship program that will start on May 18th and conclude on August 7th 2026.

What Now

Were always looking for solution-oriented critical thinkers.

So if youre 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.

#LI-HybridBlank

This position is hybrid you will be expected to work on site at one of Sareptas facilities in the United States and/or attend Company-sponsored in-person events from time to time.

The targeted salary range for this position is $21 - $26 per hour depending upon years of education completed and nature of role.

Candidates must be authorized to work in the U.S.

Sarepta Therapeutics offers a competitive compensation and benefit package.

Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.

Required Experience:

Intern

Why Sarepta Why Now The promise of genetic medicine has arrived and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle central nervous system and cardiac 2023 we launched our fourth thera...
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Key Skills

  • Laboratory Experience
  • Vendor Management
  • Design Controls
  • C/C++
  • FDA Regulations
  • Intellectual Property Law
  • ISO 13485
  • Research Experience
  • SolidWorks
  • Research & Development
  • Internet Of Things
  • Product Development

About Company

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We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.

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