Gene Therapy Potency Co-op

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 QC Potency Team at Sarepta Therapeutics is seeking a motivated and detail-oriented co-op student to join our team. This position offers a unique opportunity to gain hands-on experience in a cutting-edge biotechnology environment, working alongside experts in the field of gene therapy. This individual will support quality control testing conducted at the Sarepta Andover facility. As a co-op, you will directly contribute to the quality control processes that are essential for the release and stability of clinical and commercial products. Your work will help ensure that our therapies meet the highest standards, ultimately impacting the lives of patients with rare diseases.

The Opportunity to Make a Difference

This application is for a 6-month co-op program that will start on July 7th, 2025, and conclude on December 19th, 2025. This is a full-time, 40 hours a week, co-op program.

• Learn and assist in the execution of cell-based potency assays to test gene therapy products.
• Gain hands-on experience in performing test methods in compliance with current Good Manufacturing Practices (cGMP).
• Maintain clear and concise laboratory records in accordance with Good Documentation Practices (cGDP).
• Support reagent preparations and other related duties under the guidance of experienced team members.
• Assist in troubleshooting and optimizing test methods as needed, learning from experienced professionals.
• Conduct data analysis and data trending to support clinical and commercial lot release and stability activities.
• Collaborate with team members to gain experience on handling quality events, including deviations, CAPAs, and Change Controls.
• Spend approximately 70% of your time working in the lab and 30% on documentation, data analysis, and team meetings.
  
  

More About You

• Undergraduate (Junior or Senior) or graduate student pursuing a degree in Biology, Biochemistry, Biotechnology, or other life-science related field.
• Hands-on experience with cell culture, SDS-PAGE, and Western blot assays is a plus.
• Strong attention to detail and excellent organizational skills.
• Ability to work effectively in a team-oriented environment.
• Strong written and verbal communication skills.
• Familiarity with cGMP and cGDP is a plus.
  
  

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 requires work on site at one of Sarepta’s facilities in the United States.

The targeted salary range for this position is $22 - $34 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.