Research Assistant

Title: QC Analyst II

Location: Memphis, TN 38118

Duration: 06+ months (possibility of extension)

Shift: Monday through Friday 8:00am to 4:30pm (overtime as needed)

NOTE: Training 1 month or orientation on day shift Mon-Fri 8am – 5pm

Virtual Interview

Basic Summary

• The QC Analyst II role requires strong attention to detail, excellent organizational skills, computer proficiency, and a foundational understanding of laboratory instrumentation.
• The ideal candidate must also demonstrate effective communication skills and the ability to thrive in a fast-paced, highly technical laboratory environment.

Essential Duties and Responsibilities

• Perform cell-based immunological in vitro assays (e.g., MLR, cytotoxicity, HLA restriction, CTLp, cell proliferation, etc.) and operate related instrumentation
• Apply knowledge of cGMP/GLP regulations and maintain accurate, compliant documentation to support Quality Control activities
• Review QC test results for accuracy, precision, and compliance, ensuring timely completion of documentation aligned with product release timelines
• Conduct data analysis, including study design, statistical evaluation, and preparation of written and oral reports/presentations
• Record observations and results in trending databases for ongoing analysis and performance monitoring
• Perform aseptic techniques and support mammalian cell culture activities, including maintenance and handling of cell lines
• Support QC operations through inventory management, documentation control, log maintenance, and filing
• Participate in quality improvement initiatives and assist with laboratory investigations, including OOS, CAPA, and related quality events
• Ensure adherence to Standard Operating Procedures (SOPs) and Good Documentation Practices (GDP) to maintain data integrity and traceability
• Perform additional duties as assigned

Qualifications

• Bachelor’s degree in Biological Sciences or a related field preferred
• 1–2 years of relevant experience in a laboratory, biotech, cell therapy, or related industry; or an equivalent combination of education and experience
• Hands-on experience with aseptic technique and mammalian cell culture required
• Familiarity with cGMP regulations as defined in 21 CFR 210 and 211
• Experience with cell-based assays and molecular biology techniques preferred
• Strong attention to detail with excellent written and verbal communication skills
• Ability to work independently as well as collaboratively within a team environment