Gene Therapy Manufacturing Sciences and Technology Intern

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. 

Program Timeline

This application is for a 12-week summer internship program that will start on May 19th and conclude on August 8th, 2025.

The Importance of the Role 

Sarepta is seeking a motivated Intern for the summer of 2025 to join the Gene Therapy Manufacturing Sciences and Technology (GTMSAT) group.  As an integral member of the group, the intern will contribute to group objectives that include data compilation and process improvement initiatives. The intern will contribute towards providing process performance and comparability assessments using statistical methods. As a commercial MSAT intern, you will have the opportunity to learn about processes and controls used for production of gene therapies in GMP setting. This includes exposure to manufacturing batch records creation, investigation of unplanned deviations and technical transfer process.

You’ll be joining an organization where people of all backgrounds and experiences are respected, and where we work together focused on making a difference in the lives of our patients. In this role you’ll be reporting to the MSAT Principal Engineer.

The Opportunity to Make a Difference 

• Technical data compilations for trend assessments associated with manufacturing operations, improvements, or process change implementation initiatives
• Cross-functional team investigation of manufacturing deviations 
• Ability to apply scientific principles and statistical analysis in-order to assess process performance, identify, and solve processing issues, and evaluate opportunities for or assess the outcome of process improvements. 
• Ability to work under general supervision
• Team-orientated and proactive attitude with excellent written and communication skills
• Willingness to work collaboratively in a team-oriented environment and present information to various stakeholders
• Familiarity with and knowledge of mammalian or bacterial cell cultures and biologics production. 
• A solid understanding of statistical tools such as JMP or Excel
• Process and product quality comparability assessments using statistical tools
• Contribute to continuous improvement projects aimed at enhancing manufacturing processes, reducing costs, and increasing product quality

More about You 

• Bachelor’s or Master’s degree students in Engineering, Biological or Pharmaceutical Sciences
• Ability to apply scientific principles and statistical analysis in-order to assess process performance, identify, and solve processing issues, and evaluate opportunities for or assess the outcome of process improvements. 
• Ability to work under general supervision
• Team-orientated and proactive attitude with excellent written and communication skills
• Willingness to work collaboratively in a team-oriented environment and present information to various stakeholders
• Familiarity with and knowledge of mammalian or bacterial cell cultures and biologics production. 
• A solid understanding of statistical tools such as JMP or Excel

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.

This position is hybrid, you will be expected to work on site at one of Sarepta’s 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 - $25 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.