Cell Therapy Associate (Los Angeles)

Position Overview:
We are looking for a hands-on Manufacturing Operations Technician to contribute to the production of advanced cell-based therapies, including CAR-T and TCR-T products. This role will play a key part in executing manufacturing activities in a regulated environment while supporting readiness for clinical production. The position requires working in controlled cleanroom settings and collaborating with cross-functional teams to ensure timely and compliant manufacturing operations.

Key Responsibilities:
Execute manufacturing processes in accordance with established procedures and regulatory standards within a GMP-controlled environment
Prepare and maintain cleanroom spaces, ensuring proper setup of materials, tools, and automated processing systems
Operate specialized cell therapy equipment and support routine production activities
Follow strict aseptic techniques, gowning protocols, and cleaning procedures
Assist with implementation and documentation of manufacturing procedures, including SOP development and updates
Support activities related to facility and equipment readiness, including qualification and setup
Coordinate with internal teams such as Process Development and MS&T to align production with development needs
Monitor inventory levels of critical materials and ensure availability for scheduled manufacturing runs
Document activities accurately and provide updates to leadership on operational status
Contribute to deviation investigations and resolution as required
Participate in technology transfer activities for new or updated processes

Required Qualifications:
High School Diploma with 5+ years of relevant manufacturing experience, or a Bachelor’s degree in a science or engineering field
Practical knowledge of GMP environments and regulatory expectations for biologics manufacturing
Experience working in cleanroom settings with exposure to aseptic processing techniques
Familiarity with general manufacturing equipment and production workflows

Preferred Experience:
Background in cell therapy or biologics manufacturing
Hands-on experience with equipment such as automated cell counters, cell processing systems, and sterile welding/sealing tools
Involvement in CAR-T or similar immunotherapy production environments
Exposure to deviation handling and GMP documentation practices

Additional Skills & Expectations:
Ability to work independently and manage assigned tasks with minimal supervision
Strong problem-solving skills with the ability to address complex operational challenges
Effective planning and organizational skills in a fast-paced production setting
Clear communication skills for both written documentation and verbal updates
Readiness to contribute immediately with minimal onboarding or training