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.
The Importance of the Role
This individual will be a member of the local quality team that supports preclinical and clinical gene therapy research functions. This individual will be responsible for assisting with the maintenance of the local archives, electronic, paper, and other records.
The Opportunity to Make a Difference
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Assist with organizing, tracking, correcting, filing, and cataloging records.
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Assist with generation and updating tracking spreadsheets for various records.
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Assist with the transfer of archive records to their new location.
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Assist with the setup, inventory, and organization of the archive area.
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Assist with compiling data for internal reporting.
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Any other tasks as assigned by the Compliance team.
More about You
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Associate’s degree in a technical, administrative, or library field is desired
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Experience in a quality role in a GCLP, GLP, or cGMP environment is desired
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High proficiency in Microsoft Excel is required
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Experience in records retention/archiving is preferred
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Ability to multi-task and adapt quickly to a changing environment
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.
#LI-Onsite
This position requires work on site at one of Sarepta’s facilities in the United States.
Top Skills
What We Do
Sarepta Therapeutics, headquartered in Cambridge, Massachusetts, is a global biotechnology company on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. 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. Our vast pipeline is driven by our multi-platform Precision Genetic Medicine Engine in gene therapy, RNA and gene editing.
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