Scientific Quality Control Analyst

IntelliPro Group; North Carolina; On-site; USD 35,000 - 49,000; Part time

Job summary

IntelliPro Group in Research Triangle Park, NC seeks a Quality Control Analyst I for a 11/09/2026 to 11/07/2027 contract, on-site. The role tests non-clinical rAAV vector lots using qPCR, ddPCR, ELISA, HPLC and endotoxin methods to support release and development.

Bachelor’s degree in biology required; 0–3 years in analytical testing and tech transfer preferred; ELN experience a plus. The analyst will document procedures, review data, and participate in investigations.

Qualifications

• Bachelor’s degree in biology or related field.
• 0-3 years of analytical testing, development, and technology transfer; rAAV/gene therapy experience is a plus.

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.

Skills

Analytical testing

Data analysis

Documentation

Education

Bachelor’s degree in biology or related field

Tools

qPCR

ddPCR

ELISA

HPLC

Endotoxin testing

Electronic Laboratory Notebook

Job description

Job Title: Quality Control Analyst I

Location: Research Triangle Park, NC 27709

Position Type: Contracted - 11/09/2026 - 11/07/2027

Job Type: 100% On-site

Pay rate: $30.48/-hr on W2.

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 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 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.

Minimum Requirements:

• Bachelor’s degree in biology or related field.

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.