Position Summary

The purpose of the Analyst I, Quality Control (Non-Clinical) is to perform analytical testing to support the release of Non-Clinical grade rAAV vector lots manufactured in various client departments (including Pre-Clinical Manufacturing, Process Development, MSAT) and external partners. The rAAV vectors tested/characterized by the team will support capsid technology development, intellectual property portfolio, and internal progression of early-stage gene therapy programs.

Job Responsibilities

Perform routine and complex execution of molecular biology and biochemistry analytical methods such as qPCR, d/ddPCR, ELISA, HPLC, endotoxin etc.

Organize and perform data analysis at completion of each test method, peer review data.

Assist with the evaluation of analytical results and final reports.

Follow SOPs and document analytical test method procedures.

Assist with revisions of work instructions, SOPs, forms, reports, and electronic laboratory notebook analytical records.

Contribute to technical discussions and investigations.

Assist with the management of raw materials, analytical test method supplies, and samples as needed.

Ensure lab areas are clean, organized and equipment, supplies and raw materials are available for use.

Minimum Requirements

Bachelor's degree in biology or related field.

Preferred Education, Experience and Skills

Relevant work experience (0-2 years) in areas such as, analytical testing, development, and technology transfer; in rAAV/gene therapy, recombinant protein/biomolecules, and/or other advanced therapeutic modalities.

Experience with electronic laboratory notebooks is a plus.