Cell Therapy Specialist – Contract (Full-Time, 4/10 Schedule)
Training Requirement:
All contractors must work
Mon–Fri, 7:30 AM–4:00 PM
for the first
6–8 weeks
to complete New Hire Orientation and Manufacturing Onboarding. After training, shift assignment will be determined by department leadership. 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) About the Role
Join our Cell Therapy Manufacturing team at a
new, state-of-the-art commercial facility in Frederick, MD . As a Cell Therapy Specialist, you will execute GMP manufacturing operations, follow batch records/SOPs, and work closely with Materials Management, QC, and QA to support commercial production. Key Responsibilities
Operate, monitor, clean, and prepare automated cell processing, expansion, and filling equipment in
Grade B/C clean rooms . Troubleshoot equipment and processing issues and communicate findings to management. Complete all required cGMP training assignments. Author or revise SOPs to support compliant and efficient operations. Identify opportunities for process improvements and support deviations, investigations, and change controls. Wear full PPE and respirators when required (company provided). Basic Qualifications
Bachelor’s degree
in a Life Sciences field, OR Associate’s degree
+ 1 year of biotech experience, OR High school diploma
+ 2 years of
cGMP experience
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Mon–Fri, 7:30 AM–4:00 PM
for the first
6–8 weeks
to complete New Hire Orientation and Manufacturing Onboarding. After training, shift assignment will be determined by department leadership. 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) About the Role
Join our Cell Therapy Manufacturing team at a
new, state-of-the-art commercial facility in Frederick, MD . As a Cell Therapy Specialist, you will execute GMP manufacturing operations, follow batch records/SOPs, and work closely with Materials Management, QC, and QA to support commercial production. Key Responsibilities
Operate, monitor, clean, and prepare automated cell processing, expansion, and filling equipment in
Grade B/C clean rooms . Troubleshoot equipment and processing issues and communicate findings to management. Complete all required cGMP training assignments. Author or revise SOPs to support compliant and efficient operations. Identify opportunities for process improvements and support deviations, investigations, and change controls. Wear full PPE and respirators when required (company provided). Basic Qualifications
Bachelor’s degree
in a Life Sciences field, OR Associate’s degree
+ 1 year of biotech experience, OR High school diploma
+ 2 years of
cGMP experience
#J-18808-Ljbffr