1

Cell Therapy Process Development Jobs in Tennessee

Cell Therapy Lab Technician This Lab Technician role plays a vital part in the production of ... Contribute to validation activities and continuous improvement initiatives to enhance process ...

New

Be Seen First

Provide support in validation efforts related to the manufacturing process. * Participate in all ... Zero to 1 year of applicable experience in biotech or cell therapy. * May consider less education ...

New

Familiarity with oncology, cell therapy, transplant immunology, or immune engineering platforms preferred. * Experience contributing to early technology or platform development preferred. What They ...

Be Seen First

Biomanufacturing Technician

Memphis, TN · On-site

$20 - $22.12/hr

Provide support in validation efforts related to the manufacturing process. Participate in all ... Zero to 1 year of applicable experience in biotech or cell therapy. May consider less education and ...

New

Occupational Therapy Assistant

Jackson, TN · On-site

$24.75 - $33.25/hr

Program Development: Get involved in clinical and program development initiatives. Leadership ... cell phones, and much more! For benefit details check us out here Eligibility for some benefits ...

Be Seen First

... processing).  Write, under supervision, GMP required documents including standard operating ... cell therapy.  May consider less education and professional experience upon successful ...

New

Occupational Therapist

Jackson, TN · On-site

$38.25 - $50.25/hr

We can offer a stable and fun in-house therapy team to work with as well as excellent programs ... Program Development: Get involved in clinical and program development initiatives. Leadership ...

next page

Showing results 1-20

Cell Therapy Process Development information

What are the key skills and qualifications needed to thrive as a cell therapy process development professional?

To thrive in Cell Therapy Process Development, you need a solid background in cell biology, biotechnology, or a related field, often supported by a relevant degree and experience with cell culture techniques. Familiarity with bioprocessing equipment, Good Manufacturing Practice (GMP) regulations, and analytical tools such as flow cytometry and PCR is typically required. Strong problem-solving skills, attention to detail, and effective teamwork enhance performance in this collaborative and innovative environment. These competencies ensure the safe and efficient development of cell therapies, meeting rigorous quality standards and advancing clinical applications.

What are some typical challenges faced by professionals in cell therapy process development, and how are they addressed?

Professionals in Cell Therapy Process Development often encounter challenges such as scaling up production processes from laboratory to clinical or commercial scale while maintaining product quality and consistency. Additional hurdles include adhering to strict regulatory requirements and managing complex collaborations across cross-functional teams, like quality assurance, regulatory affairs, and manufacturing. These challenges are typically addressed through rigorous process optimization, thorough documentation, and ongoing communication with stakeholders to ensure that all aspects of the process meet industry standards and regulatory expectations.

What is the difference between Cell Therapy Process Development vs Cell Therapy Manufacturing Specialist?

AspectCell Therapy Process DevelopmentCell Therapy Manufacturing Specialist
CredentialsTypically requires a degree in biology, biochemistry, or biomedical engineering; certifications in GMP or cell therapy are commonSimilar credentials; often holds degrees in related fields and GMP certifications
Work EnvironmentResearch labs, development facilities, early-stage process optimizationManufacturing plants, production floors, quality control labs
Industry UsageFocuses on developing and optimizing cell therapy processesInvolved in large-scale production and process execution

Cell Therapy Process Development professionals focus on designing and refining cell therapy procedures, while Cell Therapy Manufacturing Specialists handle the production and quality assurance in manufacturing settings. Both roles require similar educational backgrounds and certifications but differ mainly in their work environment and specific responsibilities.

What is cell therapy process development?

Cell Therapy Process Development refers to the design, optimization, and scaling up of manufacturing processes for cell-based therapies, such as CAR-T cells or stem cell products. Professionals in this field work on translating laboratory research into reproducible, efficient, and safe production methods that meet regulatory standards. This involves working with cell culture techniques, bioreactors, quality control, and process validation to ensure that therapies can be produced consistently for clinical and commercial use. The goal is to develop robust processes that deliver safe and effective cell therapies to patients.
Infographic showing various Cell Therapy Process Development job openings in Tennessee as of August 2026, with employment types broken down into 68% Full Time, and 32% Part Time. Highlights an 100% In-person job distribution.

Cell Therapy Lab Technician

Actalent

Memphis, TN • On-site

$21 - $24/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

New


Job description

Job Title: Cell Therapy Lab Technician

Job Description

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.

Essential Skills

  • 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.

Additional Skills & 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.

Job Type & Location

This is a Contract to Hire position based out of Memphis, TN.

Pay and Benefits

The pay range for this position is $21.00 - $24.00/hr.

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 & vision • Critical Illness, Accident, and Hospital • 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)

Workplace Type

This is a fully onsite position in Memphis,TN.

Application Deadline

This position is anticipated to close on Aug 21, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.


Actalent logo

About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

Social media