Cell Therapy Lab Technician

About the role

This Lab Technician role plays a vital part in the production of cutting-edge cellular therapies. The position suits individuals with a strong foundation in scientific principles and hands-on experience or a strong interest in cell culture techniques and aseptic processing within a fast-paced, regulated environment focused on innovation and quality. You will work in a GMP-regulated setting, gaining exposure to ISO Class-7 cleanroom operations, SOP authorship, deviation reporting, and client-facing tech transfer support.

Responsibilities

• Perform aseptic manufacturing activities in compliance with established procedures and maintain required aseptic qualifications.
• Support the production, formulation, and banking of cellular products in accordance with Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP) standards.
• Assist in drafting, reviewing, and updating GMP documentation, including standard operating procedures (SOPs) and batch records.
• Contribute to validation activities and continuous improvement initiatives to enhance process robustness and product quality.
• Participate in raw material handling, including receipt, verification, preparation, and storage of materials used in cell therapy manufacturing.
• Perform cell culture operations following established laboratory and sterile technique protocols.
• Maintain cleanroom standards and behaviors, including proper gowning, aseptic practices, and adherence to contamination control procedures.
• Operate and monitor laboratory instrumentation and equipment used in biomanufacturing processes, following applicable regulatory and safety guidelines.
• Document all activities accurately and timely in batch records, logs, and other controlled documents in alignment with regulatory expectations.
• Communicate effectively with cross-functional teams to support tech transfer, troubleshooting, and process optimization activities.
• Follow all safety procedures when working with biological and hazardous materials, including blood, tissues, needles, and specialized lab equipment.
• Perform additional duties as assigned to support overall manufacturing operations and organizational goals.

Requirements

• 0–1 year of experience in biotechnology or cell therapy; relevant internship experience may be considered.
• Foundational knowledge of aseptic technique and sterile processing in a laboratory or cleanroom setting.
• Familiarity with cell culture techniques and cell biology concepts.
• Basic understanding of microbiology, chemistry, biochemistry, and biology.
• Ability to work in a regulated environment following GMP and GDP standards.
• Proficiency in algebraic math to support calculations for formulations, dilutions, and process parameters.
• Strong attention to detail and organizational skills to ensure accurate documentation and compliance.
• Effective written and verbal communication skills for documentation and cross-functional collaboration.
• Demonstrated professionalism and ability to maintain confidentiality.
• Comfort working in cleanroom environments with exposure to hazardous and medical materials.
• High school diploma or equivalent required.

Qualifications

• Associate or bachelor’s degree in a scientific field such as biology, biotechnology, chemistry, biochemistry, or related discipline strongly preferred.
• Experience or coursework in biotechnology, cell biology, or related laboratory sciences.
• Familiarity with Good Manufacturing Practice (GMP), Good Documentation Practice (GDP), and relevant regulatory expectations.
• Knowledge of ISO standards and experience working in ISO Class-7 or similar cleanroom environments.
• Experience with batch record completion, review, and deviation reporting.
• Exposure to formulation activities and validation processes in a regulated environment.
• Comfort using laboratory instrumentation and equipment in a biomanufacturing or cell therapy setting.
• Understanding of personal protective equipment (PPE) requirements and safe handling of biological materials.
• Interest in continuous improvement and learning within the biotech and pharmaceutical industries.
• Ability to support client-facing tech transfer activities in a professional and collaborative manner.

Pay

The pay range for this position is $21.00 - $24.00 per hour.

Benefits

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental, and vision insurance
• Critical Illness, Accident, and Hospital insurance
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short- and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation, or Sick Leave)

Schedule

This is a Contract to Hire, fully onsite position based in Memphis, TN.