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Cell Therapy Associate

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Infotree Global Solutions

Santa Clarita, CA (In Person)

Full-Time

Posted 5 days ago (Updated 2 days ago) • Actively hiring

Expires 6/5/2026

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Job Description

Cell Therapy Associate at Infotree Global Solutions Cell Therapy Associate at Infotree Global Solutions in Valencia, California Posted in about 20 hours ago.
Type:
full-time
Job Description:
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

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