
Cell Therapy Manufacturing Specialist - GMP Operations / CAR-T Production)
Pyramid Consulting, IncRole Overview
Pyramid Consulting, Inc is hiring a mid-level Cell Therapy Manufacturing Specialist - GMP Operations / CAR-T Production). This is a contract role in Frederick. Part of Pyramid Consulting, Inc's Qa hiring, posted 3 weeks ago. The posted range is $52k to $67k. Full responsibilities, required qualifications, and the apply link are listed in the description below.
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Job Description
Immediate need for a talented Cell Therapy Manufacturing Specialist – GMP Operations / CAR-T Production). This is a 06 months contract opportunity with long-term potential and is located in Frederick, Maryland(Onsite). Please review the job description below and contact me ASAP if you are interested.
Job ID: 25-95009
Pay Range: $25 - $32/hour. Traveler benefits as per agency package. (Benefits vary by vendor and assignment.)
Key Responsibilities:
- Execute and verify GMP manufacturing activities following approved SOPs and batch records
- Operate automated cell processing, cell expansion, and fill/finish systems in classified cleanrooms
- Author, revise, and improve SOPs, manufacturing records, and controlled GMP documents
- Perform aseptic operations in Grade B/C cleanroom environments
- Support troubleshooting, deviations, investigations, CAPA, and change controls
- Collaborate cross-functionally with QA, QC, MSAT, and Manufacturing teams
- Identify opportunities for process optimization and manufacturing efficiency improvements
- Maintain inspection-ready documentation and compliance with cGMP standards
Key Requirements and Technology Experience:
- Key skills; GMP manufacturing
- SOP authoring/revision
- Cell therapy or biologics production
- Deviation investigations
- Cleanroom operations
- Bachelor’s Degree in Life Sciences, Biotechnology, Biology, or related field
- Associate’s Degree + 1+ year biotech/GMP experience
- High School Diploma + 2+ years cGMP manufacturing experience
- Cell therapy / CAR-T manufacturing
- Biologics manufacturing
- SOP authorship or document revisions
- Batch record review
- Deviation/CAPA support
- Automated manufacturing systems
- GMP cleanroom operations
Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
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Frequently Asked Questions
How do I apply for the Cell Therapy Manufacturing Specialist - GMP Operations / CAR-T Production) position at Pyramid Consulting, Inc?
Use the Apply button above to submit your application directly to Pyramid Consulting, Inc. Most applications take less than 5 minutes if your resume and contact details are ready, and you'll be routed to the employer's official application system to finish.
Where is the Cell Therapy Manufacturing Specialist - GMP Operations / CAR-T Production) position at Pyramid Consulting, Inc located?
This position is based in Frederick. Pyramid Consulting, Inc has not indicated remote or hybrid options for this role, so candidates should plan for on-site work.
How much does the Cell Therapy Manufacturing Specialist - GMP Operations / CAR-T Production) role at Pyramid Consulting, Inc pay?
Pyramid Consulting, Inc has posted a compensation range of $52k to $67k for this position. Final offers typically vary based on candidate experience, location, and internal salary bands.
When was the Cell Therapy Manufacturing Specialist - GMP Operations / CAR-T Production) role at Pyramid Consulting, Inc posted?
This role was posted on May 14, 2026 (25 days ago). It's still listed as actively hiring; we re-confirm openings against the source system multiple times per day and remove closed roles.
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