Jobs at Capricor Therapeutics, Inc.

Lead U.S. HCP marketing for a cell therapy launch: develop brand strategy, omnichannel HCP campaigns, compliant promotional materials, speaker/peer programs, field enablement, cross-functional alignment, budget management, and KPI-driven optimization to drive awareness and adoption among neuromuscular specialists and DMD care teams.

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.

Design, implement, and maintain LAN/WAN/WLAN infrastructure and security for office and lab environments. Configure Cisco and Palo Alto devices, support segmented lab/manufacturing networks, ensure regulatory compliance and validation readiness, monitor performance with tools like SolarWinds, support cloud networking (AWS/Azure), maintain audit-ready documentation, and participate in incident response and change management.

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 MSAT Training Specialist II/III develops and delivers GMP training programs, mentors staff, maintains regulatory documentation, and ensures compliance 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 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 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 QC Specialist, Analytical ensures compliance with cGMP standards by leading investigations, reviewing data, supporting audits, and collaborating across functions to maintain product quality.

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

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

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 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.

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

Perform routine cGMP manufacturing tasks for cell therapies including media preparation, mammalian cell culture, documentation, inventory/cleanroom management, SOP and CAPA activities, data collection, and support for deviations and investigations.

Plan and execute GxP internal and supplier audits, document findings, manage CAPAs, support inspection readiness, perform gap assessments, and collaborate with QA/QC, Manufacturing, Regulatory, Supply Chain, and IT to strengthen quality systems and SOPs.

Manage, investigate, and resolve deviations, non-conformances, and CAPAs across manufacturing, lab, and clinical operations. Perform root cause analyses and risk assessments, maintain compliant documentation, lead Deviation Review Board meetings, support audits, update SOPs, train staff, and drive continuous improvement.

Lead QA and quality systems for clinical and commercial biotech operations. Build and maintain QMS and eQMS, ensure GMP/FDA/ICH compliance, drive inspection readiness, manage audits/CAPA, support regulatory submissions and cross-functional quality risk management.