×
Register Here to Apply for Jobs or Post Jobs. X

Cell Therapy Manufacturing Associate

Job in Frederick, Frederick County, Maryland, 21701, USA
Listing for: Infotree Global Solutions
Seasonal/Temporary position
Listed on 2025-12-17
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer
Salary/Wage Range or Industry Benchmark: 27 - 32 USD Hourly USD 27.00 32.00 HOUR
Job Description & How to Apply Below

Infotree Global Solutions Provided Pay Range

This range is provided by Infotree Global Solutions. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base Pay Range

$27.00/hr - $32.00/hr

Job Summary

We are seeking a driven Cell Therapy Specialist to join our commercial manufacturing team. In this role, you will play a key part in producing innovative cell therapy products by performing manufacturing activities under cGMP standards. The position involves hands‑on work in clean rooms, operation of advanced cell processing equipment, and close collaboration with Quality, Materials Management, and other cross‑functional teams. This is an exciting opportunity to contribute directly to our mission of curing cancer.

Key Responsibilities
  • Perform and document manufacturing operations in accordance with batch records, SOPs, and cGMP requirements.
  • Operate, monitor, and maintain automated cell processing, expansion, and filling systems in classified cleanroom environments.
  • Troubleshoot technical and process issues, escalating and collaborating with management as needed.
  • Author and revise SOPs, ensuring alignment with compliance standards and operational efficiency.
  • Complete all required training to maintain cGMP knowledge and technical expertise.
  • Support investigations, deviations, and continuous improvement initiatives to enhance compliance and productivity.
Education Qualification
  • Bachelor’s degree in a science‑related discipline; or
  • Associate’s degree with 1+ years of cGMP experience; or
  • High school diploma with 2+ years of cGMP experience.
Required Experience
  • Background in cell therapy, biologics, or pharmaceutical GMP manufacturing.
  • Strong aseptic technique and cleanroom gowning experience.
  • Familiarity with automated cell processing platforms (e.g., MACSQuant).
  • Knowledge of GMP, GLP, or GCLP regulations and compliance standards.
  • Excellent problem‑solving, communication, and organizational skills.
  • Flexibility to work varied shifts (Day or Swing; 4/10 schedule) as directed by department needs.

Seniority level:
Associate

Employment type:

Contract

Job function:
Manufacturing

Industries:
Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

#J-18808-Ljbffr
Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary