The individual will conduct GMP QC release and stability testing using state of art Quantitative Polymerase Chain Reaction, qPCR, Droplet Digital PCR (ddPCR) and Sequencing (Sanger and NGS).

The candidate should have hands on experience of viral DNA manipulation and quantification methods and. All aspects of this position involve working in a GMP compliant manner.

This position requires occasional coverage late evening and a few hours on a weekend.

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 qualification and supply to external sites.
• Author and resolve / close Quality Events (deviations, CAPAs, investigations, change controls, etc.) promptly and on-time.
• Trend data for qualified materials, release products, and stability products
• Create and maintain clear and concise lab records and documentation.
• Expected to spend 80% in laboratory testing and 20% combination of meetings and documentation.
• Perform other related duties incidental to the work described.

Desired Education and Skills :

• B.S. degree in molecular biology or cell biology
• QC Associate I / II : 0 2 years relevant experience
• Working experience in a cGMP environment is desired.
• A strong understanding of qPCR, ddPCR, and knowledge of DNA Sequencing (Sanger and NGS) is desired.
• Self-starter with the ability to work in a fast-paced, cross-functional, highly collaborative environment.
• Experience with EpMotion liquid handling system, Quant Studio, Droplet generator and Droplet readers is useful.
• Experience in general laboratory experimentation and electronic documentation is necessary.
• Must have effective written and verbal communication skills.
• Attention to details is a must.
• Operate as part of a team, assisting fellow lab associates in providing a functional, safe working environment while maximizing laboratory efficiency.

LI-Onsite

This position requires work on site at one of Sarepta’s facilities in the United States.

The targeted salary range for this position is $72,000 - $90,000 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.

Last updated : 2024-05-14