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You will be updated with latest job alerts via emailWhy 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 limbgirdle 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.
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 Opportunity to Make a Difference
This application is for a 6month coop program that will start on July 7th 2025 and conclude on December 19th 2025. This is a fulltime 40 hours a week coop program.
Support cGMP manufacturing investigations statistical data analysis and rootcause analysis and implement continuous improvement initiatives to improve process robustness.
Utilize a variety of technological platforms (i.e. JMP Power BI Microsoft 365 Suite) and collaborate across disciplines (i.e. Process Development Quality Assurance Validation Regulatory Affairs Manufacturing) to develop a latestage technology transfer dashboard to enable efficiency and knowledge transfer.
Opportunity to travel to Contract Manufacturing Organization and support largescale cGMP Gene Therapy Upstream/Downstream Person in Plant (PiP) to gain valuable insight into our manufacturing processes and bring learnings internally to better our portfolio.
Analyze compile and present results to internal and cross functional teams comprised of members from multiple groups and stakeholders.
More about You
Undergraduate (junior or senior) or graduate student pursuing a degree in chemical engineering biomedical engineering or a related discipline.
Interest and/or experience in data science Power BI dashboard development project management and exposure to GMP manufacturing suites.
Experience in biotechnology/gene therapy specifically drug substance process development and manufacturing.
Advanced knowledge and/or laboratory experience in gene therapy cell culture and purification methods.
Maintain a strong work ethic and good documentation practices including electronic laboratory notebook maintenance and writing of technical reports and SOPs
Ability to multitask learn new skills and possess flexibility that is needed in a fastpaced team environment.
What Now
Were always looking for solutionoriented 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.
Full-Time