Capricor Therapeutics Jobs in United States

The Senior Director, Quality Assurance & Quality Systems provides strategic and operational leadership for all quality activities supporting Capricor's clinical-stage and advancing commercial-stage organization. · $210,000 - $270,000 a year · ...

The Quality Systems Specialist is responsible for supporting Capricor's transition to the Veeva electronic Quality Management System (eQMS) and providing ongoing system administration configuration and maintenance. · ...

The Quality Control Associate for Environmental Monitoring (EM) plays a critical role in maintaining the environmental conditions required for GMP manufacturing. · Conduct routine environmental monitoring in controlled and classified areas in alignment with GMP, ISO, and regulato ...

+Job summary · Support planning coordination execution of projects across CMC GMP manufacturing commercial readiness activities for therapeutic products. · +Support GMP facility commissioning decommissioning activities. · Track program schedules metrics. · ...

Supports cGMP manufacturing operations through technical writing investigation management and process-focused scientific problem solving. · ...

The GMP Operations Supervisor plays a critical role in ensuring operational excellence and compliance within Capricor's GMP environment. · Oversee and manage GMP Operations engineers on validation best practices, execution and documentation. · Maintain and update calibration and ...

We are seeking a Science to join our Pre-Clinical team to support the progression of our therapeutic programs through the design, execution, · and optimization of in vivo research activities and preclinical studies.Partner with the Principal Scientist and Director to provide prec ...

+The Quality Systems Associate will support and maintain Capricor's Quality Management System (QMS) to ensure compliance with FDA, GMP, ISO 9001, and internal quality standards.+ · +Responsibilities · Support maintenance and continuous improvement of the Quality Management System ...

Capricor Therapeutics is seeking a Senior Director of Medical Affairs with deep expertise in biotechnology to play a pivotal role in building the medical affairs function as we advance our lead programs following recent clinical milestones. · ...

Capricor Therapeutics seeks a Director of Regulatory Affairs to provide strategic leadership in Chemistry Manufacturing Controls activities across product lifecycle. · Develop execute CMC regulatory strategy aligning with global requirements. · Oversee preparation authoring revie ...

The Supplier Quality Management (SQM) Supervisor plays a critical role in building and maintaining Capricor's world-class supplier quality program.This position oversees supplier qualifications, audit activities, supplier performance monitoring, · and compliance with global GMP r ...

+Capricor Therapeutics is a biotechnology company seeking an individual to join their Quality Compliance department. The ideal candidate will conduct internal and external audits to ensure compliance with applicable regulations and standards. · +Responsibilities include planning, ...

+ Program Management Associate will play an essential role in supporting the planning, coordination and execution of cross-functional projects. + Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and fam ...

We are looking for an exceptional individual to join our growing team as a Material Handler. The Material Handler will play a critical role in supporting our manufacturing and logistics operations by managing inventory, processing shipments, and ensuring the efficient movement of ...

We are seeking an individual to join our Quality Compliance department. This role conducts internal and external audits to ensure our biopharma operations comply with applicable regulations, standards, and company procedures. · ...

The Quality Control Associate, Lab Operations position plays an essential role in supporting daily laboratory operations within the Quality Control organization. This position ensures the QC labs are stocked, organized, safe, and compliant—directly enabling QC analysts and scient ...

Capricor Therapeutics is seeking a self-motivated team player with attention to detail who enjoys organizing, making processes better, and making a difference in patient lives. · ...

+Job summary · The Quality Control Associate plays a critical role in maintaining environmental conditions required for GMP manufacturing. · Conduct routine environmental monitoring in controlled areas. · Analyze data to identify trends... · ...

The Product Quality Specialist supports Capricor's cell therapy programs by assisting in the implementation of cGMP requirements, regulatory expectations, and industry best practices. · Ensure cGMP compliance throughout all stages of product development, including clinical and co ...

In this role, you will lead the development and continuous improvement of quality engineering processes to ensure product quality and regulatory compliance. · Lead and manage the Quality Engineering team, providing direction and mentorship. · Develop and maintain quality engineer ...