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Sarepta Jobs in Ohio (NOW HIRING)

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$8

$24

$56

How much do sarepta jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for sarepta in Ohio is $24.08, according to ZipRecruiter salary data. Most workers in this role earn between $13.84 and $28.13 per hour, depending on experience, location, and employer.

What is Sarepta?

A Sarepta job typically refers to a role at Sarepta Therapeutics, a biopharmaceutical company focused on developing precision genetic medicines, particularly for rare diseases like Duchenne muscular dystrophy. Positions at Sarepta span various fields, including research and development, clinical operations, regulatory affairs, and manufacturing. Employees at Sarepta contribute to cutting-edge therapies, working in a fast-paced and innovative environment.

What does Sarepta do?

Sarepta is not typically a job title, but rather the name of a biotechnology company, Sarepta Therapeutics, that specializes in developing precision genetic medicines for rare diseases. Employees at Sarepta work in various roles such as research, clinical development, regulatory affairs, manufacturing, and corporate operations. The company is known for its contributions to the development of treatments for Duchenne muscular dystrophy (DMD) and other genetic disorders. Career opportunities at Sarepta often require backgrounds in science, medicine, regulatory compliance, or business administration. Working at Sarepta means contributing to innovative therapies that aim to improve the lives of people with rare diseases.

What are the key skills and qualifications needed to thrive as a professional at Sarepta Therapeutics?

To thrive at Sarepta Therapeutics, professionals typically need a strong background in biotechnology, molecular biology, or related life sciences, often supported by an advanced degree or relevant industry experience. Familiarity with drug development processes, regulatory compliance systems, and laboratory technologies such as PCR and bioinformatics tools is usually required. Excellent problem-solving abilities, teamwork, and strong communication skills help employees excel in collaborative, fast-paced environments. These competencies are essential for advancing innovative therapies and ensuring the rigorous standards necessary in the biopharmaceutical industry.

What are some unique challenges faced by professionals working at Sarepta Therapeutics, and how can new hires best prepare for them?

Working at Sarepta Therapeutics, which specializes in precision genetic medicine for rare diseases, often involves navigating a fast-paced and highly regulated environment. New hires should be prepared to adapt quickly to shifting priorities due to the dynamic nature of drug development and regulatory requirements. Collaboration across multidisciplinary teams, including research, clinical, and regulatory affairs, is essential for advancing projects. Staying organized, being proactive in communication, and maintaining a patient-focused mindset can help new team members thrive in this innovative setting.

What is the difference between Sarepta vs Genetic Counselor?

AspectSareptaGenetic Counselor
Required CredentialsBiotech or pharmaceutical background, often with a degree in life sciencesMaster's degree in genetics or genetic counseling, certification required
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsHospitals, clinics, healthcare settings
Industry UsageDeveloping therapies, clinical trials, biotech researchPatient counseling, risk assessment, genetic testing interpretation

While Sarepta focuses on biotech research and therapy development, a Genetic Counselor primarily works directly with patients to interpret genetic information. Both roles require a background in genetics, but Sarepta is more research-oriented, whereas Genetic Counselors are patient-facing healthcare professionals.

What are popular job titles related to Sarepta jobs in Ohio?

For Sarepta jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Sarepta jobs in Ohio look for?

The top searched job categories for Sarepta jobs in Ohio are:

Sarepta jobs near you
Infographic showing various Sarepta job openings in Ohio as of August 2026, with employment types broken down into 74% Full Time, and 26% Part Time. Highlights an 86% In-person, and 14% Hybrid job distribution, with an average salary of $50,085 per year, or $24.1 per hour.

Scientist-II Developability & Preformulation

Columbus, OH

Sarepta Therapeutics
Biotechnology Research and Development • 1 - 5K employees
Learn more about Sarepta Therapeuticsexternal

Full-time

Re-posted 22 hours ago

Job description

Why Sarepta? Why Now?

The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. 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 Early Research and Process Development (ERPD) group is seeking a Scientist II with experience in biologics preformulation and developability assessment, with a focus on proteins, antibodies, and antibody-oligonucleotide conjugates (AOCs). This individual will support the assessment of developability for lead molecules through comprehensive evaluations, including biophysical characterization, forced degradation, and short-term, long-term, and in-use stability studies.
The successful candidate will leverage high-throughput formulation tools and workflows to characterize product stability across a broad range of conditions, including process buffers, excipients, concentrations, hold times, and temperatures. In collaboration with Analytical Development, the candidate will help define quality attributes and implement stability-indicating assays appropriate for early-stage programs. The Scientist II will also consider route-of-administration factors, such as subcutaneous delivery, during early formulation assessments (e.g., stability and viscosity at high concentrations, potential enabling approaches).
This role requires strong cross-functional engagement, working closely with Upstream and Downstream Process Development, High-Throughput Automation, and CMC Drug Substance/Drug Product teams to foster a collaborative environment that enables the advancement of robust and scalable manufacturing processes. The Scientist II will contribute formulation recommendations to research, pilot-scale, and commercial-scale manufacturing groups and generate scientifically rigorous data packages to inform preclinical and early clinical development and enable downstream CMC strategy for Sarepta's genetic therapy engine.
Sarepta provides a creative culture that invites you to be the best that you can be and is committed to making a difference in patient's lives. Join us at the Genetic Therapy Center of Excellence here in Easton, Ohio.

The Opportunity to Make a Difference

    • Plan and execute formulation experiments to assess andoptimizethe stability of key intermediates and final products throughout the manufacturing process.

    • Establish developability profiles for candidate molecules, incorporating considerations for route-of-administration.

    • Identifyformulation-relevant critical quality attributes for key intermediates and drug productcandidates andguide the development of stability-indicating assays tomonitorthem.

    • Contribute scientific recommendationsregardingformulation technologies and instrumentation.

    • Support cross-functional teams by providing recommendations on product handling and storage considerations.

    • Prepare and review methods, protocols, and technical reports for regulatory submissions or technology transfer.

    • Train and support Research Associates in experimental execution, troubleshooting, and data interpretation.

More about You

  • Degree in Biochemistry, Biochemical Engineering, Bioengineering, or Chemical Engineering

  • Ph.D. with3-5yearsor M.S. with6-8yearsof biologics formulation experience,

  • Experience withbiologicsformulation(e.g.,mAbs) isrequired. Experience withAOCs or antibody-drug conjugates (ADCs)formulationis a plus.

  • Hands-on experience with protein formulation technologies(e.g., Unchained Labs Big Tuna/Big Kahuna/Junior, Sartorius AMBR Crossflow,Pendotech5TFF, Repligen KR2i, etc.).

  • Experience with stability and analytical assaystomonitorproduct quality, including SEC,RP, CE-SDS,cIEF,DLS, DSF, MALS,and mass spectrometry.

  • Experience with high-concentration formulation challenges (e.g., viscosity mitigation strategies, excipient screening, protein-protein interaction understanding)

  • Experience applying Design of Experiments (DoE) principles to formulation development is a plus.

  • Demonstrated ability to work effectively in cross-functional teams and communicate scientific findings to internal stakeholders.

  • Proficiencyin statistical or data analysis tools (e.g., JMP, GraphPad,SigmaPlot) is a plus.

  • Prior experience in therapeutic protein discovery or biochemistry research.

  • Excellent written and verbal communication skills.

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-OnsiteThis position requires work on site at one of Sarepta's facilities in the United States.The targeted salary range for this position is $106,400 - $133,000 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.

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