QC Laboratory Analyst - 26-00173

LeadStack Inc.; Durham (NC); On-site; USD 38,572 - 41,328; Full time

Job summary

A leading consulting firm is seeking a QC Analyst I to perform critical GMP testing and maintain laboratory documentation. Candidates must have a Bachelor’s degree in biology or a related field, with experience in analytical testing and SOP compliance. Responsibilities include conducting analytical testing, preparing solutions, and collaborating with development and quality control teams. The position offers hourly compensation between $28 and $30 on a W2 basis, reflecting the importance of maintaining high-quality laboratory standards.

Qualifications

• Experience with ddPCR and qPCR testing.
• Familiarity with laboratory documentation and data management.
• Ability to prepare laboratory solutions and maintain cell lines.

Responsibilities

• Perform routine analytical testing and maintain lab documentation.
• Prepare solutions and maintain cell lines as needed.
• Assist with revisions and ensure compliance with SOPs.

Skills

Analytical testing

GMP testing

Documentation maintenance

Cell-based potency assays

HPLC techniques

Education

Bachelor’s degree in biology or related field

Job description

Locations: Research Triangle Park, NC 27709

PR: $28/hr to $30/hr on W2

Position Summary

The QC Analyst I, reporting to the Manager of Quality Control, will be responsible for performing routine GMP testing on analytical methods in the Quality Control laboratories.

Job Responsibilities

• Perform routine analytical testing including but not limited to cell-based potency assays, ddPCR, qPCR, ELISAs, limit tests using HPLC techniques.
• Prepare solutions and maintain cell lines for various clinical programs.
• Prepares laboratory solutions, maintains cell lines, and other day to day laboratory activities.
• Maintains laboratory documentation including logbooks, test forms, LIMS data, and electronic data.
• Assist with revisions of work instructions, SOPs, forms, reports, and electronic laboratory notebook analytical records.
• Assist with management analytical test method supplies and samples as needed.
• Ensure lab areas are clean, organized, maintain equipment and consumables.
• Work closely with Analytical Development, Quality Control, Quality Assurance, Production staff and any other relevant departments.
• Strictly adheres to all applicable written Standard Operating Procedures (SOPs), company policies, and technical guidance documents, both internal and external.
• Participates in continuous improvement projects in the AD and QC labs.
• Support revisions to work instructions, SOPs, forms, protocols, and reports.
• Bachelor’s degree in biology or related field.