Default company background
Sarepta Therapeutics

Sarepta Therapeutics in United States

42 jobs at Sarepta Therapeutics in United States


  • Sarepta Therapeutics Massachusetts, United States

    The MSL will play a pivotal role in the education of healthcare professionals (HCPs) about Duchenne Muscular Dystrophy and Limb Girdle Muscular Dystrophy as well as Sarepta's investigational therapeutics and product pipeline. · Reporting to the East Region Team Leader, the MSL po ...


  • Sarepta Therapeutics Cambridge, United States

    This position will be responsible and accountable for leading the Global Program Team (GPT) to create and execute an integrated development strategy which coherently integrates the clinical, non‐clinical, regulatory, medical affairs, manufacturing, commercial, and market access p ...


  • Sarepta Therapeutics Andover, United States

    Primary Responsibilities Include: · - Perform Quantitative Polymerase Chain Reaction, qPCR and Droplet Digital PCR (ddPCR), Sequencing (Sanger and NGS) in support of release and stability testing of AAV based gene therapy products. · - Support activities related to viral control ...


  • Sarepta Therapeutics Cambridge, United States

    The Director, Clinical Development is responsible for leading a clinical sciences team responsible for advancement of Sarepta's clinical-stage programs. The individual is responsible for defining strategic priorities for the program and integrating cross-functional input in order ...


  • Sarepta Therapeutics Cambridge, United States

    The Manager, Forecasting will be responsible for supporting commercial forecast development to support the commercial success of Sarepta's current platform and other pipeline products. This position will partner with key stakeholders (Competitive Intelligence teams, Market Access ...


  • Sarepta Therapeutics Burlington, United States

    The Senior Manager, Capital Projects operates within the Real Estate, Facilities and Engineering department. This position develops facility projects (lab, office and Current Good Manufacturing Practice (cGMP) Manufacturing), both renovation and new construction, to support the S ...


  • Sarepta Therapeutics Andover, United States

    This individual will join the Analytical Development team involved in the development of novel AAV Gene Therapy analytical methods. The individual will have an in-depth knowledge of AAV gene therapy analytical methods that include qPCR, ddPCR, TCID50, rcAAV, SDS-PAGE, CE, ELISA, ...


  • Sarepta Therapeutics Andover, United States

    The Sarepta Therapeutics QA Compliance Unit is seeking to fill a Full-Time position for Manager, Quality Engineer to develop and maintain GxP quality systems processes and procedures to drive quality compliance and business efficiencies. Develop and maintain processes to facilita ...


  • Sarepta Therapeutics Andover, United States

    The Executive Director QC leads a high-functioning QC group comprising 35-40 individuals and 3 direct reports. The ideal candidate should be highly skilled in managing external manufacturing and testing sites both in the USA and across the world. The successful candidate will fos ...


  • Sarepta Therapeutics Cambridge, United States

    The Data Scientist, Research Sciences role at Sarepta is an exciting opportunity for someone with strong data science and analytical skills who wants to see their work directly impacting patient care. In this hands-on role, the data scientist will research and develop advanced an ...


  • Sarepta Therapeutics Burlington, United States

    Intern will learn overview of parenteral pharmaceutical business & industry. Emphasis will be learning and understanding of drug product distribution systems and maintaining product integrity to deliver products to pharmacies, clinics, and hospitals to dispense product. Intern wi ...


  • Sarepta Therapeutics Andover, United States

    The QA Senior Associate is responsible for batch record review and disposition of clinical and commercial lots. The Senior Associate will be a key member of QA team in the assessment of CMO batch compliance with FDA and ICH regulations as well as internal procedures. This person ...


  • Sarepta Therapeutics Cambridge, United States

    Serves as a stat programming expert or point of contact for assigned clinical studies under close/limited supervision of the stat programming project lead · Primary Responsibilities Include: · • Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and ...


  • Sarepta Therapeutics Cambridge, United States

    The Senior Manager, Regulatory Affairs CMC supports RA CMC gene therapy development product(s) and provides support for Chemistry, Manufacturing and Controls (CMC) Regulatory Affairs. They will work closely with subject matter experts within CMC technical operations and QA workin ...


  • Sarepta Therapeutics Cambridge, United States

    The Director, Competitive Intelligence will manage the Customer organization's competitive intelligence function. This includes maintaining timelines, industry knowledge, market alerts, conference coverage, primary market research, and Leadership briefings on competitive events a ...


  • Sarepta Therapeutics Cambridge, United States

    Co-lead the strategy and implementation of global regulatory strategies for In Vitro Diagnostics (IVD)/Companion Diagnostics (CDx) to support business objectives. Act as the interface with multiple internal and external stakeholders, including partners. Works as Global Regulatory ...


  • Sarepta Therapeutics Massachusetts, United States

    The MSL will play a pivotal role in the education of healthcare professionals (HCPs) about Duchenne Muscular Dystrophy and Limb Girdle Muscular Dystrophy as well as Sarepta's investigational therapeutics and product pipeline. · Reporting to the East Region Team Leader, the MSL po ...


  • Sarepta Therapeutics Cambridge, United States

    The Associate Director of Finance - Inventory and Manufacturing Operations will be responsible for managing the execution of processes aimed at delivering performance-based analytics within the Technical Operations organization. Key duties include managing the product costing pro ...


  • Sarepta Therapeutics Cambridge, United States

    Co-lead the strategy and implementation of global regulatory strategies for In Vitro Diagnostics (IVD)/Companion Diagnostics (CDx) to support business objectives. Act as the interface with multiple internal and external stakeholders, including partners. · Works as Global Regulato ...


  • Sarepta Therapeutics Columbus, United States

    Job Description Summary: Entry Level Technician - Executes simple tasks as directed, very limited scope for independent tasking and judgement. · •Works on problems of limited scope, under established guidelines or supervision. · •Follows standard practices and procedures in mai ...