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MOI​/QCCB Lead Operator

Job in Raritan, Somerset County, New Jersey, 08869, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-10-06
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly USD 90000.00 130000.00 YEAR
Job Description & How to Apply Below
Role

MOI/QCCB Lead in manufacturing autologous CAR-T cell therapy within a cGMP environment, focusing on Multiplicity of Infection and Quality Control Cell Bank processes.

Responsibilities
  • independently execute manufacturing and support activities such as cell culturing, purification, aseptic processing, cryopreservation
  • ensure compliance with SOPs, batch records, and GDP
  • support process development and continuous improvement
  • maintain safe, compliant work environment
  • contribute to audit readiness and investigation efforts
Requirements
  • HS diploma with 6+ years biotech/pharma experience or Bachelor's in Life Sciences/Engineering with 2+ years industry experience
  • basic knowledge of manufacturing systems, GMP, and process documentation
  • ability to operate lab and manufacturing equipment
  • strong documentation and data entry skills
High Value
  • Cell therapy (CAR-T)
  • autologous process
  • cGMP
  • process development
  • manufacturing operations
  • quality compliance
  • documentation
  • team collaboration
Work Setup

Location:

Raritan, NJ

Working hours:

Monday–Friday
Physical demands include mobility, lifting up to 25 lbs, gowning, and working in sterile environments.

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