Quality Control Analyst

About the Role

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 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.

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 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 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.

Requirements

• Bachelor’s degree in biology or related field.

Qualifications

Preferred Education, Experience, and Skills:

• Relevant work experience (0-3 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.

Pay

$22/hr – $31/hr on W2

Location: Research Triangle Park, NC – 27709 | Duration: 12 Months Contract