New

Research Associate I HTPA

Sarepta Therapeutics
United States, Ohio, Columbus
Mar 16, 2025
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. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas: Physical and Emotional Wellness Financial Wellness Support for Caregivers For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us The Importance of the Role The Research Associate (RA) I, high throughput process automation (HTPA), will utilize automation workflows and robotic liquid handlers to execute experiments for the development and optimization of downstream processes. They will additionally be responsible for performing experiments supporting the development of automated high throughput analytical assays for deployment by the Analytical Development team. They will be expected to support these process development activities by generating reliable and reproducible data with thorough documentation. They will operate in a highly collaborative environment within HTPA, but will also work closely with the Upstream Process Development, Downstream Process Development, Analytical Development, and Vector Core groups towards the collective goal of early research process development to produce sound and robust manufacturing processes for AAV vectors. The Opportunity to Make a Difference Operate laboratory automation equipment (e.g. Tecan) to support high throughput process development experiments using a variety of high throughput chromatography techniques Support the development of high throughput analytical assays Support the creation of high throughput tools and workflows Participate in lab management activities including the preparation of laboratory reagents, maintenance of laboratory instrumentation, and ordering of laboratory materials Analyze, collate, track, and report data back to stakeholders Work independently and efficiently Document work clearly and perform tests accurately Communicate results effectively with stakeholders Contribute to a safe, efficient, and effective environment with personal accountability More about You Bachelor's degree in Biology, Biochemistry, Bioengineering, Chemical Engineering, Biomedical Engineering, or a related field is required with 1-3 years of related experience Basic laboratory skills (buffer making, pipetting, weighing, etc.), with at least 1 year of laboratory experience Experience in downstream processing techniques for production of biologics and viral vectors highly preferred Experience working with laboratory automation or advanced laboratory equipment such as Aktas or robotic liquid-handlers preferred Experience in programming/coding (e.g. equipment software, Visual Basic, C++, MatLab, Python, etc.) considered a plus Strong computer, scientific, and organizational skills Excellent written and verbal communication skills Proven ability to work independently as well as part of a team, and effectively handle multiple priorities is a must 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 Blank This position requires work on site at one of Sarepta's facilities in the United States. The targeted salary range for this position is $60,800 - $76,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta's compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. 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.