Jobs at Capricor Therapeutics, Inc.

Maintain day-to-day workplace functionality, safety, and professionalism by monitoring office and lab-adjacent areas; coordinate facilities, security, and vendors; manage visitor check-in and badges; oversee parking and site coordination; support events, onboarding logistics, and room setups; ensure safety/compliance and escalate facility issues.

Support development and maintenance of analytical workflows and dashboards for biological and manufacturing datasets. Perform data extraction, cleaning, integration, and QC for transcriptomics and proteomics. Assist with RNA-seq/proteomics preprocessing, generate figures/tables, document reproducible workflows, and support cloud and database organization while collaborating with R&D, Manufacturing, Quality, and Data Science teams.

Supervise a cGMP biologics manufacturing team to ensure compliant execution of cell culture, formulation, and freezing operations. Oversee documentation, batch records, deviations/CAPAs, training, inventory, cleanroom activities, process monitoring, and cross-functional coordination to meet quality and production goals.

Lead development and scale-up of closed-system adherent cell culture processes to improve yield, quality, and cost. Design and run experiments, mentor junior scientists, manage project teams, evaluate technologies, and collaborate with MSAT, manufacturing, quality, and regulatory to translate discoveries into validated, compliant processes.

Lead scale-up and optimization of adherent cell culture bioprocesses using bioreactors and closed systems. Design and execute experiments, solve manufacturing challenges, mentor junior scientists, and collaborate with MSAT, manufacturing, quality, and regulatory teams to translate research into validated, GMP-compatible processes.

The role involves conducting audits to ensure compliance with regulations in biopharma operations, documenting findings, and supporting continuous improvement initiatives.

The Quality Control Scientist ensures product quality in cell therapies by optimizing methods, validating processes, and complying with regulatory standards, while supporting cross-functional teams.

The Supplier Quality Management Manager oversees the supplier quality program, audits, and compliance with GMP regulations while ensuring high standards in supplier qualifications and corrective actions.

The Quality Control Scientist will lead analytical control material development, oversee QC assay strategies, and ensure regulatory compliance by managing assay lifecycle activities and collaboration with multiple teams.

The Manufacturing Associate I performs routine manufacturing tasks, mentors team members, manages documentation, and leads quality assurance initiatives in a GMP environment.

Join Capricor Therapeutics' Preclinical Team to conduct in vivo studies, optimize methodologies, and ensure compliance with regulations for therapeutic programs.

The Quality Control Associate II will generate and maintain control materials for QC testing, perform analytical assays, and support method optimization. They will collaborate with scientists and ensure documentation is compliant with GMP standards.

The Director of Commercial Operations & Analytics will lead the launch operations, sales analytics, and CRM ecosystem for Deramiocel, a cell therapy. Responsibilities include building teams, setting operational frameworks, and ensuring alignment across departments for commercial success.

Manage the commercial launch program, ensuring cross-functional alignment and operational excellence, while optimizing processes and tracking progress.

The MSAT Associate 2 supports cGMP operations through technical writing, investigation management, and process-focused problem solving in cell therapy manufacturing.

The Senior Systems Engineer will design, implement, and support enterprise IT infrastructure, ensuring the systems are secure and scalable in a biotech environment.

The QC Specialist, Analytical ensures compliance with cGMP standards by leading investigations, reviewing data, supporting audits, and collaborating across functions to maintain product quality.

The Director leads quality assurance and quality systems activities in biotechnology, ensuring compliance with regulatory standards and managing cross-functional collaborations.

The Quality Assurance Associate II aids in batch record reviews, document management, internal audits, and ensures compliance with cGMP regulations in a biotechnology environment.

The MSAT Training Specialist II/III develops and delivers GMP training programs, mentors staff, maintains regulatory documentation, and ensures compliance in cell therapy manufacturing.