What are the responsibilities and job description for the Cell Therapy (Manufacturing Specialist) position at Cube Hub Inc.?
Job Title: Cell Therapy (Manufacturing Specialist (GMP)
Location: Tarzana, CA (Onsite; occasional travel to Santa Monica, CA)
Duration: 03 Months (Contract/Temp with the possibility of extension)
Shift: 1st Shift
Pay Range: $23/hr to $25/hr
Schedule: Monday–Friday, 8 hours/day (may transition to 4x10 schedule: Sun–Wed or Wed–Sat)
Job Description:
We are seeking an experienced Manufacturing Specialist to support cell therapy production within a dynamic and fast-paced biopharmaceutical environment. This role focuses on the manufacturing of investigational products such as CAR-T, TCR-T, and allogeneic cell therapies in compliance with cGMP standards.
This is a hands-on role requiring cleanroom operations, equipment handling, and strict adherence to quality and regulatory guidelines.
Key Responsibilities:
Support GMP readiness activities including equipment procurement, installation, qualification, and facility readiness
Perform manufacturing operations in a cleanroom/aseptic environment following cGMP standards
Set up and operate complex cell therapy manufacturing equipment
Follow all gowning, cleaning, and contamination control procedures
Assist in development and revision of Standard Operating Procedures (SOPs)
Maintain inventory of materials and ensure availability for production activities
Support technology transfer and alignment between Manufacturing, Process Development (PD), and MSAT teams
Ensure all production activities meet regulatory and compliance requirements
Document and communicate manufacturing updates and deviations
Perform additional project-based tasks as needed
Required Qualifications:
High School Diploma with 5 years of relevant experience OR Bachelor’s degree in Life Sciences, Engineering, or related field
Experience working in a cGMP-regulated environment
Hands-on experience with aseptic techniques and cleanroom operations (ISO 5 preferred)
Knowledge of cell culture and biologics manufacturing processes
Understanding of CMC and GMP regulatory frameworks
Preferred Qualifications:
Experience in cell therapy manufacturing (CAR-T, TCR-T, or similar)
Familiarity with equipment such as: Nucleocounter (NC-200), Sepax, Sefia, Finia, Cell processing systems, welders, sealers, microscopes
Experience supporting tech transfer and clinical manufacturing
Exposure to deviation investigations and documentation
Salary : $23 - $25