Manufacturing Technician

Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We also harness our proprietary StealthX platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most. Responsibilities Maintaining cleanroom inventory, performing material transfers and cleanroom-required activities to support cGMP operations (i.e restocking Kanban, scrubs, and gowning) Ensuring clear communication and working closely with manufacturing and materials management to confirm proper materials are stocked accordingly Performing cleanroom setup and shutdown (Biohazard waste decontamination, packaging and autoclaving of required materials/supplies, etc.) Performing special manufacturing projects Completing required documentation with proper cGMP recording of entries and comments on batch records, forms and protocols independently Operation, Maintenance, and Cleaning of GMP equipment, including: Centrifuges, Microscopes, Incubators, BSCs, Refrigerators, Freezers, etc. Initiate minor revisions to existing documents, to troubleshoot simple existing procedures, and to contribute to continuous improvement initiatives Perform such other duties as may be assigned from time to time Qualifications High school diploma or GED required Lift, push, pull and carry up to 40 lbs. Excellent knowledge of aseptic technique and aseptic practices Exceptional communication and interpersonal skillsExcellent organizational skills and attention to detail Excellent interpersonal skills, team player Ability to work in a dynamic environment Adaptable/flexible with work schedule with an ability to multi-task and prioritize work From time-to-time extended hours may be required with or without notice, dependent on the work needed Occasional weekend work may be required Preferred Qualifications Bachelor’s degree in Biology, Biological Sciences or related field preferred 1+ years of experience in GMP/cGMP manufacturing environment in academic/industry setting Excellent knowledge of Good Documentation Practices #J-18808-Ljbffr