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Cell Therapy Technician

Job in Urbana, Frederick County, Maryland, USA
Listing for: The Fountain Group
Full Time position
Listed on 2026-01-01
Job specializations:
  • Manufacturing / Production
    Operations Engineer, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 30 - 34.75 USD Hourly USD 30.00 34.75 HOUR
Job Description & How to Apply Below
Position: Cell Therapy Technician I*
Location: Urbana

Pay rate is $30.00-$34.75 per hour
Cell Therapy Manufacturing Technician – cGMP (Frederick, MD)

Full-Time | 4/10 Schedule | Multiple Shifts Available

Overview

Join a state-of-the‑art commercial Cell Therapy facility driven by one mission:
curing cancer. Our Frederick, MD site is expanding its Cell Therapy Manufacturing team and seeking a highly motivated Cell Therapy Technician to support commercial manufacturing operations. This role is essential to producing cutting‑edge, life‑changing immunotherapies for patients.

Important Training Requirement

For the first 6–8 weeks
, all contractors must work Monday–Friday, 7:30 AM–4:00 PM to complete New Hire Orientation and Technical Manufacturing Onboarding.
Upon successful completion of this training, technicians will transition to an assigned shift based on operational needs.

Shift Structure (Post-Training) – 4/10 Schedule

Shift assignments may change based on department needs. Managers or department leads will determine the specific schedule.
Day Shift (6:00 AM–4:30 PM): Sun–Wed or Wed–Sat
Swing Shift (3:00 PM–1:30 AM): Sun–Wed or Wed–Sat

Key Responsibilities
  • Perform and/or verify all activities associated with the manufacturing of commercial cell therapy products following batch records and cGMP‑compliant SOPs
    .
  • Operate, monitor, and maintain sophisticated automated cell processing, cell expansion, and filling equipment within Grade B/C cleanroom environments.
  • Execute GMP production runs in collaboration with Materials Management, Quality Control, and Quality Assurance
    .
  • Troubleshoot process and equipment issues, escalating appropriately to management.
  • Complete all required training to maintain technical proficiency and ensure compliance with cGMP and internal quality standards.
  • Support deviation investigations, change controls, and continuous improvement initiatives to enhance manufacturing efficiency and compliance.
  • Perform routine cleaning, preparation, and operation of equipment; follow gowning and PPE requirements for classified cleanroom areas.
  • Wear a respirator when applicable for specific cleaning procedures.
  • Contribute to a culture grounded in safety, compliance, teamwork, and a shared mission of curing cancer.
Basic Qualifications
  • High School Diploma + 1+ year of relevant experience
    , OR
  • Associate’s Degree + 0+ years of relevant experience
  • Experience with cell therapy or mammalian cell culture in a cGMP manufacturing environment is required.
  • Candidates without cGMP cell therapy/cell culture experience will not be considered.
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