Associate I, Quality Control Technical Services

$60,000 - $75,000/Yr

Sarepta Therapeutics - Andover, MA

Full-time - Entry Level

Andover, MA

Chemical Manufacturing

About the position

The Associate I, Quality Control Technical Services role at Sarepta Therapeutics focuses on providing qPCR and ddPCR assay support for AAV-based gene therapy products. This position involves interacting with subject matter experts (SMEs) and assisting in the development, qualification, and validation of analytical methods, while conducting laboratory tests to support regulatory filings and clinical comparability.

Responsibilities

• Perform Quantitative Polymerase Chain Reaction (qPCR) and Droplet Digital PCR (ddPCR) based test methods in support of in-process, release, stability, and investigative testing of AAV based gene therapy products.
• Assist with the development, qualification, and validation activities related to viral test methods (qPCR & ddPCR) for AAV based gene therapy products intended for clinical and commercial stage programs.
• Troubleshoot routine technical challenges and contribute to their resolution.
• Create and maintain clear and concise lab records and documentation.
• Perform other related duties incidental to the work described.

Requirements

• B.S. degree in Molecular Biology, Microbiology, Biology, Chemistry or related field with 0 - 2 years relevant experience.
• Strong understanding of contemporary molecular biology methods with hands-on qPCR experience is required.
• Experience with ddPCR, liquid handling automation systems (epMotion), and QuantStudio PCR systems is useful.
• Experience working in a cGMP environment is desired.
• Experience in general laboratory experimentation and documentation is required.
• Effective written and verbal communication skills and strong attention to detail are necessary.
• Ability to operate as part of a team, assisting fellow lab associates in providing a functional, safe working environment while maximizing laboratory efficiency.

Nice-to-haves

• Experience with ddPCR and liquid handling automation systems (epMotion) is useful.
• Experience working in a cGMP environment is desired.

Benefits

• Comprehensive benefits package including physical and emotional wellness support.
• Financial wellness resources.
• Support for caregivers.