Capricor Therapeutics is a biotechnology company focused on the development of transformative cell and exosome-based therapeutics for the treatment of rare diseases. Founded in 2005, Capricor is dedicated to advancing innovative regenerative medicine solutions to address unmet medical needs. With a strong emphasis on research and development, Capricor Therapeutics is committed to improving patient outcomes and making a meaningful impact in the field of healthcare.

<div><span style="font-size: 16px;">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&nbsp;</span><b style="font-size: 16px;">Deramiocel&nbsp;</b><span style="font-size: 16px;">(</span><i style="font-size: 16px;">CAP-1002</i><span style="font-size: 16px;">), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</span></div><div><br></div><div><span style="font-size: 12pt;">We are seeking an experienced </span><b style="font-size: 12pt;">EQMS Business Analyst with specialized expertise in Veeva Vault</b><span style="font-size: 12pt;">, preferably someone who has led or played a key role in </span><b style="font-size: 12pt;">full Vault implementations (QualityDocs, QMS, Training, and other Vault Quality modules)</b><span style="font-size: 12pt;">. The ideal candidate will bridge business needs with system capabilities, ensuring that our Veeva ecosystem supports compliant, efficient, and scalable quality operations.</span></div>

EQMS Business Analyst – Veeva Vault (Full Vault Implementation)

<div><span style="font-size: 16px;">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&nbsp;</span><b style="font-size: 16px;">Deramiocel&nbsp;</b><span style="font-size: 16px;">(</span><i style="font-size: 16px;">CAP-1002</i><span style="font-size: 16px;">), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</span></div><div><br></div><div><span style="font-size: 16px;">The Supplier Quality Associate is a critical role responsible for overseeing the development and maintenance of a robust supplier quality program, managing external audit programs, and ensuring compliance with Good Manufacturing Practice (GMP) standards. This position will drive supplier qualifications, conduct risk-based audits, and collaborate with cross-functional teams to maintain high-quality standards and support continuous improvement. The ideal candidate is a detail-oriented professional with extensive experience in supplier quality management and GMP/GLP environments, capable of working independently to meet project goals while ensuring regulatory compliance. This role will play a pivotal part in upholding Capricor’s commitment to quality and excellence in the development of innovative therapies.</span></div><div><span style="font-size: 16px;">The team this person will be joining develops and maintains the Supplier Quality Program, conducts supplier qualifications and audits, manages SCAR activities, generates and manages Quality Agreements, and develops SOPs.</span></div>

Supplier Quality Associate

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The Post-Marketing Product Quality Compliance Manager will oversee post-market product quality activities in compliance with FDA regulations and internal Quality System requirements. This role leads and develops a team responsible for product quality complaints, post-distribution quality monitoring, and the execution of quality-driven field actions, including recalls and market withdrawals. The manager provides strategic direction, coaching, and performance management to ensure timely, compliant, and effective execution of post-market quality processes while fostering a culture of quality and continuous improvement.</div>

Post-Marketing Quality Compliance Manager

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div><span style="font-size: 16px">As a Manufacturing Associate I, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success.</span></div><div><br></div><div><br></div>

Manufacturing Associate I

<div>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 are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>Capricor is seeking a self-motivated team player with attention to detail, who enjoys organizing, making processes better, and making a difference in patient lives.&nbsp; The Quality Assurance QA Associate II – Quality Events Team (QET) is responsible for cross-functional triage of issues and managing, investigating, and resolving deviations, non-conformances, and corrective and preventive actions (CAPAs) in compliance with cGMP, SOPs, and regulatory requirements. This role ensures the consistent application of quality standards across manufacturing, laboratory, and clinical operations while supporting continuous improvement initiatives. The position will report to the Manager of Quality Assurance.&nbsp;</div><div><br></div><div>Position: Quality Assurance Associate II- Quality Events Team (Hybrid) 2nd shift, 3pm-1130pm</div>

Quality Assurance Associate II- Quality Events Team

<div><span style="font-size: 16px;">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&nbsp;Deramiocel&nbsp;(</span><i style="font-size: 16px;">CAP-1002</i><span style="font-size: 16px;">), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</span></div><div><br></div><div><span style="font-size: 16px;">As a GCP Specialist, you will support GCP compliance for clinical operations to ensure regulatory adherence. You will assist in compliance processes and collaborate with cross functional teams to maintain clinical trial integrity.</span></div>

GCP Specialist

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>We are seeking a driven and detail-oriented Facilities Associate II / III to support and lead GMP facility operations. This individual will be responsible for independently managing equipment calibration and maintenance programs, coordinating complex vendor activities, and contributing to continuous improvement initiatives across facilities and compliance systems. The ideal candidate brings hands-on GMP experience, demonstrates sound judgment in a regulated environment, and takes initiative in solving operational issues. This role is based at our headquarters in San Diego, CA.</div>

Facilities Associate II / III

<div>The GMP Operations Supervisor plays a critical role in ensuring operational excellence and compliance within Capricor’s GMP environment. This position is responsible for managing and executing equipment validation, calibration and preventive maintenance schedules, coordinating vendor activities, and supporting facilities operations to uphold the highest standards of quality and regulatory compliance. The ideal candidate is detail-oriented, proactive, and thrives in a fast-paced, dynamic setting where precision and collaboration are key.</div>

GMP Operations Supervisor

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><p>The QC Specialist, Analytical supports the quality and compliance of cell therapy programs through a focus on data review, investigations, and quality systems. This role plays a key part in ensuring that QC methods, analytical data, and documentation meet cGMP requirements and regulatory expectations for clinical and commercial manufacturing.&nbsp;Working cross-functionally with Quality Assurance, Analytical Development, and Manufacturing, this position emphasizes technical writing, data analysis, and product quality oversight. While maintaining a strong understanding of laboratory operations, the role is not primarily focused on routine bench work.</p>

Quality Control Specialist, Analytical

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The GMP Operations Engineer plays a critical role in ensuring operational excellence and compliance within Capricor’s GMP environment. This position is responsible for executing equipment validation protocols, managing equipment calibration and preventive maintenance schedules, coordinating vendor activities, and supporting facilities operations to uphold the highest standards of quality and regulatory compliance. The ideal candidate is detail-oriented, proactive, and thrives in a fast-paced, dynamic setting where precision and collaboration are key.</div>

Operations Engineer II/III

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>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 materials within our facilities. This role requires attention to detail, a commitment to quality, and the ability to work effectively in a fast-paced environment.</div><div><br></div><div>Operations run between <b>6:00 AM–6:00 PM</b>, with roles assigned to one of two set shift windows: <b>6:00 AM–2:30 PM</b> or <b>9:30 AM–6:00 PM</b>. Openings are distributed across locked weekly schedules—<b>Sat–Wed, Tue–Sat, Thu–Mon, and Fri–Tue</b>—and you will be hired into one of these specific schedules. While shifts do not rotate, candidates should maintain flexibility for <b>1–2 hours of overtime as needed</b> to support production and shipping demands.</div>

Material Handler I

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The Associate I/II, Regulatory Operations will provide essential regulatory operations and document management support across Capricor’s development and potential commercial programs. This role is primarily responsible for tracking regulatory deliverables, maintaining document repositories and archives, and assisting with submission readiness, publishing, and lifecycle management activities. The Associate will collaborate closely with Regulatory Affairs, CMC, Clinical, Quality, Manufacturing, and other cross-functional teams to ensure regulatory documents are complete, accurate, current, and readily available to support BLA submissions, regulatory interactions, and ongoing compliance in a fast-paced biotech environment.</div>

Associate I/II, Regulatory Operations

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The <b>Director, CMC Regulatory Affairs</b> provides strategic leadership and ownership of Chemistry, Manufacturing, and Controls (CMC) regulatory activities across Capricor’s product lifecycle, with primary accountability for Deramiocel’s BLA pathway and advancement of other pipeline candidates from development through potential commercial approval and post-approval maintenance. Reporting to and collaborating closely with the VP of Regulatory Affairs, this role develops and executes CMC regulatory strategy, ensures compliance with global requirements (FDA, ICH, EMA), identifies and mitigates risks, and partners with cross-functional teams (CMC Development, Manufacturing, Quality, MSAT, Supply Chain, and others) to drive successful submissions, health authority interactions, and company objectives in a fast-paced, mission-driven biotech environment.</div>

Director, CMC Regulatory Affairs

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The <b>Manager, CMC Regulatory Affairs</b> is responsible for executing Chemistry, Manufacturing, and Controls (CMC) regulatory activities across Capricor’s product lifecycle, with a primary focus on supporting the BLA pathway for Deramiocel and advancing other pipeline candidates from development through potential commercial approval and post-approval maintenance. This role supports the development and implementation of CMC regulatory strategy, ensures compliance with global regulatory requirements (including FDA, ICH, and EMA guidelines), and partners closely with cross-functional teams (e.g., CMC Development, Manufacturing, Quality Assurance, Clinical, and Regulatory) to enable timely submissions, successful interactions with health authorities, and achievement of company objectives in a dynamic biotech environment.</div>

Manager, CMC Regulatory Affairs

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The Senior Director, Quality Assurance &amp; Quality Systems provides strategic and operational leadership for all quality activities supporting Capricor’s clinical-stage and advancing commercial-stage organization. This role has full accountability for the design, execution, and continuous improvement of the Quality Management System (QMS) to ensure sustained regulatory compliance, inspection readiness, and robust quality oversight across development, manufacturing (including cell therapy production), and potential commercialization of Deramiocel and StealthX™-based programs.</div><div><br></div><div>The Senior Director partners closely with executive leadership, Regulatory Affairs, CMC, Clinical, Manufacturing, and other cross-functional teams to enable late-stage development, BLA submissions and responses (including addressing any quality-related aspects of the Deramiocel pathway), commercial readiness, and scalable growth while embedding a proactive, risk-based quality culture across the enterprise.</div>

Senior Director, Quality Assurance & Quality Systems

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The HR Coordinator at Capricor Therapeutics will serve as the central point of contact for the employee lifecycle, supporting recruitment coordination, onboarding, record maintenance, and compliance efforts in a fast-growing biotech environment. By ensuring accurate documentation, seamless coordination of HR processes, and responsive support to employees and managers, this role plays a vital part in strengthening people operations, fostering a positive and inclusive workplace culture, and enabling the company’s mission-driven growth as we advance our pipeline toward potential approvals and commercialization.</div>

Human Resources Coordinator

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The Quality Control Associate for Environmental Monitoring (EM) plays a critical role in maintaining the environmental conditions required for GMP manufacturing. This position is responsible for performing routine and specialized sampling, analyzing trends, documenting results, and ensuring controlled areas maintain compliance with regulatory and internal quality standards. As part of the QC EM team, you will perform hands-on monitoring of air, surfaces, and personnel, as well as water system and utility testing to ensure facility integrity. You will be responsible for maintaining accurate, real-time documentation and supporting investigations into any environmental excursions or anomalies. Working closely with QC, QA, and Production, this role ensures that manufacturing and testing environments remain in a constant state of control to support the production of high-quality therapeutic products.</div>

Quality Control Associate - Environmental Monitoring

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>Capricor is seeking a Manager or Senior Manager of Commercial Logistics to lead the day-to-day operational execution of commercial distribution activities for our growing portfolio. This individual will oversee GxP‑compliant logistics, cold‑chain distribution, serialization and DSCSA processes, and 3PL partnerships that support product launch readiness and ongoing commercial operations. This role is critical as Capricor transitions from clinical-stage to commercial-stage operations and scales its distribution capabilities globally.</div>

Manager / Senior Manager, Commercial Logistics

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The <b>Supplier Quality Management (SQM) Supervisor</b> 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 requirements across the supply chain. The role requires strong collaboration with Procurement, Manufacturing, QC, R&amp;D, and other functional partners to ensure that externally supplied materials and services consistently meet Capricor’s quality standards. This position is ideal for detail‑oriented quality professionals with deep experience in GMP/GLP environments and a passion for continuous improvement.</div>

Supplier Quality Management (SQM) Supervisor

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div><span style="font-size: 10.5pt;">The MSAT Associate 2 supports cGMP manufacturing operations through technical writing, investigation management, and process-focused scientific problem solving. This role requires a strong understanding of cell therapy or&nbsp;biologics&nbsp;manufacturing and a demonstrated ability to analyze data, manage quality events, and provide real-time support to production activities.&nbsp;</span></div><div><br></div><div><span style="font-size: 10.5pt;">In this position you will act as a Subject Matter Expert (SME) across manufacturing processes, supporting technology transfer, continuous improvement, deviation investigations, and the development and revision of controlled documentation. This position partners closely with Manufacturing, QA, Process Development, and Supplier Quality to ensure compliant, efficient, and well‑documented operations.&nbsp;</span></div>

MSAT Associate 2

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>We are seeking a <b>Science</b> to join our <b>Pre-Clinical</b> team to support the progression of our therapeutic programs through the design, execution, and optimization of in vivo research activities and preclinical studies. This role requires deep expertise in in vivo methodologies, strong technical skills, and the ability to perform complex operations in a regulated environment.</div>

Scientist – Preclinical Team

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>We are seeking an experienced <b>NetSuite Administrator</b> to manage, maintain, and optimize our NetSuite ERP system within a regulated pharmaceutical environment. This role is critical to ensuring system integrity, GxP compliance, audit readiness, and adherence to SOX/internal control requirements.</div><div>The ideal candidate brings deep NetSuite expertise combined with experience operating in FDA-regulated or compliance-heavy environments. This individual will serve as the subject matter expert for NetSuite and partner cross-functionally with Finance, IT, Quality, and Operations to drive scalable, compliant solutions.</div>

NetSuite Administrator

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>We are seeking a detail-oriented and highly motivated <b>Senior Accountant</b> to join our growing finance team. This role will play a key part in supporting core accounting functions, including general ledger management, fixed assets, prepaids, and construction-in-progress (CIP). The ideal candidate is a collaborative team player who thrives in a dynamic, fast-paced environment and is eager to contribute to a meaningful mission.</div>

Senior Accountant

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>Capricor is seeking Senior Director of Medical Affairs with deep expertise in biotechnology, ideally in rare diseases or cell therapies. This position will play a pivotal role in building the medical affairs function as we advance our lead programs following recent clinical milestones. This individual will define the roadmap for our scientific narrative, drive clinical scientific messaging, foster key relationships with healthcare professionals (HCPs), key opinion leaders (KOLs), and patient advocacy groups in the DMD and BMD communities, and ensure high-integrity, compliant processes for stakeholder engagement. This new headcount position supports our major milestone of positive Phase 3 results and continued advancement of deramiocel. They will lead cross-functional efforts to bridge clinical development with commercialization readiness, fostering deep relationships and evidence generation strategies necessary to drive program success and ongoing medical excellence.</div>

Senior Director, Medical Affairs

<div><span style="font-size: 16px;">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&nbsp;Deramiocel&nbsp;(</span><i style="font-size: 16px;">CAP-1002</i><span style="font-size: 16px;">), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</span></div><div><br></div><div><span style="font-size: 16px;">The License Associate III will lead and coordinate the preparation, submission, and maintenance of initial facility and establishment license applications for drug manufacturing and tissue operations in the United States, European Union, and Japan.</span></div><div><span style="font-size: 16px;">This role is pivotal in ensuring the company’s manufacturing sites and partner facilities are fully licensed and compliant with GMP (Good Manufacturing Practice), GTP (Good Tissue Practice), and regional ATMP regulatory frameworks. The successful candidate will collaborate closely with key stakeholders to support global launch readiness and regulatory compliance for advanced therapy products.</span></div>

License Associate III

<div><span style="font-size: 16px;">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&nbsp;Deramiocel&nbsp;(</span><i style="font-size: 16px;">CAP-1002</i><span style="font-size: 16px;">), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</span></div><div><br></div><div><span style="font-size: 16px;">As a Manufacturing Associate I, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success.</span></div>

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The Corporate Compliance Officer is responsible for leading, developing, and overseeing the company’s comprehensive corporate compliance program, with a primary focus on internal compliance, trade compliance, reporting requirements, document retention, quality compliance, anti-corruption, data privacy and industry standards in the pharmaceutical/biotech sector. Reporting to the Executive Vice President-General Counsel, this role partners closely with Commercial, Clinical, CMC, Quality, Regulatory, and Operations to ensure all company activities align with applicable laws, regulations, contractual obligations, and ethical standards. The ideal candidate is a seasoned compliance professional with deep pharmaceutical or biotech experience, proven leadership in building and managing compliance programs, with experience in international trade compliance involving Europe and/or Japan (e.g., export controls, sanctions, trade regulations, customs, or cross-border technology transfer).</div>

Corporate Compliance Officer

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The In‑House Legal Counsel provides broad commercial and corporate legal support for Capricor’s growing operations, with a focus on contract negotiation, vendor management, commercialization readiness, and day‑to‑day legal advisory work across the business. Reporting to the General Counsel, EVP, this role partners closely with Commercial, Clinical, CMC, Quality, Regulatory, Operations, and Finance to ensure Capricor’s activities align with applicable legal, contractual, and industry standards. The ideal candidate is a motivated junior–mid level attorney with strong law‑firm training and experience supporting pharmaceutical or biotech clients, particularly in commercial contracting and product‑launch environments.</div>

In-House Legal Counsel

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>As an Associate Director / Director of Patient Advocacy at Capricor, you will guide and advance Capricor’s U.S. patient advocacy strategy across the company’s portfolio. In this role, you will cultivate trusted, compliant relationships with patient advocacy organizations, elevate the patient voice across the enterprise, and ensure patient perspectives meaningfully inform strategy from development through commercialization. The ideal candidate brings deep experience partnering with advocacy communities, strong cross functional collaboration skills, and a commitment to patient centered impact in rare and specialty disease areas.</div>

Associate Director / Director of Patient Advocacy

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <p>The Site Support Coordinator is responsible for maintaining the day-to-day functionality, safety, and professionalism of the workplace. This role ensures the office, lab-adjacent spaces, and common areas remain organized, clean, and compliant with company policies. &nbsp;</p> <p>This individual will regularly walk the facility floors to monitor workplace conditions, support employees and visitors, and coordinate with facilities, security, and vendors to resolve issues quickly. In a small biotech environment, this role is highly visible and critical to maintaining a productive, safe, and welcoming workplace.&nbsp;</p> </div>

Site Support Coordinator

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>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. This role will assist in document control, training, audit preparation, quality records management, and system administration while collaborating across functional teams to strengthen Capricor’s quality operations.</div> <div>This is an excellent opportunity for someone who is detail‑oriented, organized, and eager to grow their quality career in a fast‑paced biotech environment.</div>

Quality Systems Associate 2

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>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 materials within our facilities. This role requires attention to detail, a commitment to quality, and the ability to work effectively in a fast-paced environment.</div> <div>&nbsp;</div> <div>Operations run between <strong>6:00 AM–6:00 PM</strong>, with roles assigned to one of two set shift windows: <strong>6:00 AM–2:30 PM</strong> or <strong>9:30 AM–6:00 PM</strong>. Openings are distributed across locked weekly schedules—<strong>Sat–Wed, Tue–Sat, Thu–Mon, and Fri–Tue</strong>—and you will be hired into one of these specific schedules. While shifts do not rotate, candidates should maintain flexibility for <strong>1–2 hours of overtime as needed</strong> to support production and shipping demands.</div>

<div> <div><span style="font-size: 16px;">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&nbsp;</span><strong style="font-size: 16px;">Deramiocel&nbsp;</strong><span style="font-size: 16px;">(</span><em style="font-size: 16px;">CAP-1002</em><span style="font-size: 16px;">), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</span></div> <div>&nbsp;</div> <div><span style="font-size: 16px;">We are seeking a meticulous and detail-oriented CSV (Computer System Validation) Engineer to join our dynamic team. The CSV Engineer will be responsible for ensuring that computerized systems used in the biopharma industry comply with regulatory requirements. This includes developing and executing validation protocols, documenting processes, acting as the business system owner, and providing technical expertise to ensure systems operate effectively and meet industry standards.</span></div> </div>

CSV Engineer II / III

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>We are seeking an experienced <strong>Veeva Vault EQMS Specialist</strong>&nbsp;with deep expertise in Veeva Vault, ideally someone who has led or played a key role in full implementations across QualityDocs, QMS, Training, and other Vault Quality modules. This role will partner closely with Quality and cross‑functional teams to translate business needs into scalable system design, ensuring that our Veeva ecosystem supports compliant, efficient, and future‑ready quality operations.</div>

Veeva Vault EQMS Specialist

<div>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&nbsp;<strong>Deramiocel&nbsp;</strong>(<em>CAP-1002</em>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div> <div>&nbsp;</div> <div>As a Manufacturing Supervisor, you will oversee the manufacturing team, ensuring cGMP-compliant production of biologic products for clinical trials. You will supervise daily operations, mentor staff, and collaborate with the Associate Director of Manufacturing to drive efficiency, quality, and regulatory adherence.&nbsp;</div>

Manufacturing Supervisor

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div><span data-contrast="auto">The Analytical Development Scientist is a senior technical contributor within the Analytical Development team. This role leads the development, optimization, and validation of complex analytical methods supporting cell therapy and biologic products, operating with a high degree of independence and scientific judgment. The Scientist takes ownership of cross-functional projects, drives assay strategy, and ensures execution aligns with regulatory expectations and program timelines. This role contributes to technical decision-making, supports advancement of programs from early development through commercialization, and provides mentorship while fostering strong collaboration across teams.</span><span data-ccp-props="{&quot;201341983&quot;:0,&quot;335551550&quot;:1,&quot;335551620&quot;:1,&quot;335559738&quot;:120,&quot;335559739&quot;:0,&quot;335559740&quot;:240}">&nbsp;</span></div>

Analytical Development Scientist - Cell Therapy

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <p>The Operations Coordinator is responsible for maintaining the day-to-day functionality, safety, and professionalism of the workplace. This role ensures the office, lab-adjacent spaces, and common areas remain organized, clean, and compliant with company policies. &nbsp;</p> <p>This individual will regularly walk the facility floors to monitor workplace conditions, support employees and visitors, and coordinate with facilities, security, and vendors to resolve issues quickly. In a small biotech environment, this role is highly visible and critical to maintaining a productive, safe, and welcoming workplace.&nbsp;</p> </div>

Operations Coordinator

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The Planning &amp; Procurement Manager leads Capricor’s end-to-end materials planning, procurement (direct and indirect), and inventory strategies to ensure uninterrupted availability of GMP materials. This role manages a multidisciplinary team including Procurement and Planning staff. A successful candidate will provide leadership, operational oversight, and strategic direction.</div> <div>&nbsp;</div> <div>&nbsp;The Manager will support Capricor’s ongoing operational growth by ensuring that planning and procurement processes scale effectively with the organization. This includes contributing to the development of future warehouse capabilities, supporting ERP enhancements, and strengthening cross-functional coordination. The Manager ensures supplier performance, planning accuracy, regulatory compliance, and alignment with Manufacturing, Quality, and Warehouse Operations.</div>

Planning and Procurement Manager

<div>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&nbsp;<strong>Deramiocel&nbsp;</strong>(<em>CAP-1002</em>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div> <div>&nbsp;</div> <div> <p style="margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 10.0pt; font-family: Arial, sans-serif;">The QA II/III is responsible for performing Quality Assurance oversight and review activities supporting donor eligibility determinations and GMP manufacturing operations for cell therapy products. This role ensures that donor-derived starting materials used for cell therapy manufacturing meet regulatory and internal quality requirements prior to use. The position supports compliance with applicable regulations including 21 CFR 1271, 21 CFR Parts 210/211, and applicable GTP/GMP guidance.</span></p> <p style="margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;">&nbsp;</p> <p style="margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 10.0pt; font-family: Arial, sans-serif;">QA II/III performs independent review of donor screening documentation, infectious disease testing results, and associated records to ensure donor suitability prior to release of starting materials for manufacturing. Donor eligibility determinations represent a critical quality decision affecting the suitability of donor-derived starting materials for use in cell therapy manufacturing.</span></p> <p style="margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;">&nbsp;</p> <p style="margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 10.0pt; font-family: Arial, sans-serif;">This role has the authority to perform QA review and approval of donor eligibility and suitability determinations in accordance with approved procedures and regulatory requirements.</span></p> <p style="margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 10.0pt; font-family: Arial, sans-serif;">In addition, the role supports routine QA Operations activities including batch record review, deviation oversight, change control support, and inspection readiness.</span></p> <p style="margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;">&nbsp;</p> <p style="margin: 0in; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 10.0pt; font-family: Arial, sans-serif;">The level of this position (QA II or QA III) will be determined based on the candidate’s experience, depth of knowledge, and demonstrated ability to independently perform donor eligibility and suitability determinations with appropriate judgment and minimal oversight.</span></p> </div>

Quality Assurance Associate II/III – Donor Eligibility & Suitability

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <p>We are seeking a highly skilled and hands-on Senior Systems Engineer to design, implement, and support enterprise IT infrastructure in a fast-paced biotech environment. This role will be responsible for maintaining highly available, secure, and scalable systems across cloud and on-prem environments.</p> <p>The ideal candidate brings deep expertise in systems engineering, cloud platforms, automation, and security, with experience operating in regulated environments (GMP, SOX, etc.).</p> </div>

Senior Systems Engineer

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <p>We are seeking a detail-oriented and service-driven IT Support Technician to support our growing biotech organization in the Torrey Pines area. This role is critical in maintaining reliable IT operations across both corporate and laboratory environments.</p> <p>You will serve as the frontline IT support resource, ensuring seamless access to systems while maintaining compliance with regulatory standards such as GMP, and FDA 21 CFR Part 11.</p> <p>This is an excellent opportunity for someone who wants to grow their IT career in a mission-driven, science-focused environment.</p> </div>

IT Support Technician

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <p>The Operations Associate II/III supports the execution of operational readiness activities across key functions, including Facilities and cross-functional operational programs. This role helps ensure day-to-day operations run smoothly by coordinating documentation, supporting operational projects, maintaining organized records, and assisting with employee onboarding and workplace logistics.</p> <p>The position partners closely with Operations, Facilities, IT, QA, Manufacturing, and EHS to support structured systems and processes that enable both GMP and non-GMP operations, as well as overall facility readiness.</p> </div>

Operations Associate II/III

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><p>The Quality Control Associate III, Sample Management is responsible for the receipt, tracking, storage, distribution, and disposal of samples in a controlled laboratory or regulated environment. This role ensures sample integrity, accurate documentation, and compliance with applicable regulatory and quality standards.</p>

Quality Control Associate III, Sample Management

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <div> <p><span data-contrast="auto">The&nbsp;</span><span data-contrast="auto">Quality Control Associate II/III, Analytical</span><span data-contrast="auto">&nbsp;will perform analytical testing to support batch disposition,&nbsp;in process&nbsp;control, drug substance and drug product release, and stability studies. This role is central to ensuring product quality and regulatory compliance for&nbsp;Capricor’s&nbsp;cell based&nbsp;and&nbsp;exosome based&nbsp;therapeutic platforms.</span><span data-ccp-props="{}">&nbsp;</span></p> </div> <div> <p><span data-contrast="auto">You will execute analytical assays,&nbsp;maintain&nbsp;mammalian cell cultures, document data in GMP&nbsp;compliant systems, support investigations, and collaborate&nbsp;cross&nbsp;functionally&nbsp;to ensure&nbsp;testing&nbsp;readiness and continuous improvement. This is a&nbsp;hands-on&nbsp;QC bench role within an expanding analytical team and a new headcount supporting pipeline and manufacturing scaleup.</span><span data-ccp-props="{}">&nbsp;</span></p> </div> </div>

Quality Control Associate II/III, Analytical

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The Warehouse Manager is responsible for overseeing all daily warehouse operations,&nbsp;including inbound receiving, inventory control, and replenishment, ensuring timely&nbsp;processing, inventory accuracy, and efficient order fulfillment to meet the needs of all&nbsp;internal and external customers.&nbsp;</div> <div>&nbsp;</div> <div>This role leads and develops a team of material handlers and team leads, Supervisor drivingperformance through adherence to company SOPs, safety standards, and operational best&nbsp;practices. The Warehouse Manager fosters a culture of accountability, continuous&nbsp;improvement, and safety-first execution.&nbsp;</div> <div>&nbsp;</div> <div>In addition, this position is accountable for monitoring and achieving key performance indicators (KPIs), leading cross-functional projects, and continuously reviewing and improving SOPs. The role partners with internal stakeholders to implement process enhancements&nbsp;through structured change control methods and leverages ERP systems to optimize&nbsp;warehouse efficiency and data accuracy to support supply planning procurement and&nbsp;meeting financial objectives.</div> <div><br>This role collaborates closely with internal stakeholders across all Supply Chain functions, as&nbsp;well as external vendors and regulatory inspectors, to support operational and business&nbsp;requirements. The Warehouse Manager ensures clear, timely communication and alignment&nbsp;across all partners to drive efficient execution and compliance.&nbsp;Additionally, this position supports and responds to both internal and external audits,&nbsp;ensuring audit readiness, accurate documentation, and timely resolution of any findings</div>

Warehouse Manager

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div><span style="font-size: 10.5pt;">The MSAT Associate 2 supports cGMP manufacturing operations through technical writing, investigation management, and process-focused scientific problem solving. This role requires a strong understanding of cell therapy or&nbsp;biologics&nbsp;manufacturing and a demonstrated ability to analyze data, manage quality events, and provide real-time support to production activities.&nbsp;</span></div> <div>&nbsp;</div> <div><span style="font-size: 10.5pt;">In this position you will act as a Subject Matter Expert (SME) across manufacturing processes, supporting technology transfer, continuous improvement, deviation investigations, and the development and revision of controlled documentation. This position partners closely with Manufacturing, QA, Process Development, and Supplier Quality to ensure compliant, efficient, and well‑documented operations.&nbsp;</span></div>

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <p>The Warehouse Lead is responsible for overseeing our warehouse operations, ensuring&nbsp;efficient operations and adherence to safety, quality, and organizational standards. The ideal&nbsp;candidate will have experience in warehouse management, a keen eye for detail, and a&nbsp;strong commitment to safety and efficiency. This role is crucial in ensuring the smooth and&nbsp;efficient operation of our warehouse, supporting our mission to deliver high-quality biotech&nbsp;products.</p> </div>

Warehouse Lead

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <p>This Warehouse Supervisor oversees daily incoming, inventory and replenishment operations&nbsp;to ensure timely receipts, accurate inventory management, organization and on time&nbsp;fulfillment to support all end users.</p> <p>This Role will manage a team of materials handlers, leads to ensure adherence to company&nbsp;SOPs and all requirements with safety alignment.&nbsp;This role will support KPIs, Projects, SOP review, updates, and process improvements through&nbsp;change controls with collaborative partners and effectively using ERP.</p> </div>

Warehouse Supervisor

<p>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&nbsp;<strong>Deramiocel&nbsp;</strong>(<em>CAP-1002</em>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</p> <p>&nbsp;</p> <div> <p><span style="font-size: 16px;">As a Manufacturing Technician, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trialscommercial production, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success.&nbsp;</span></p> <p>&nbsp;</p> <p><span style="font-size: 16px;">This role is a full time position on our Manufacturing team, this position will be a 2-2-3 work schedule.&nbsp;&nbsp;</span></p> </div>

Manufacturing Technician

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The Quality Control Scientist, Controls will lead the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will be responsible for generating and maintaining positive and negative controls, designing and executing analytical studies, and troubleshooting and optimizing analytical methods used in QC testing.&nbsp;</div> <div>&nbsp;</div> <div><span data-contrast="auto">This position plays a critical role in ensuring assay reliability, reproducibility, and regulatory compliance within the QC laboratory. The individual will provide scientific leadership for assay control strategies, oversee analytical lifecycle activities for control materials, and collaborate with Quality Control, Analytical Development, Process Development, Manufacturing, and Quality teams to ensure robust analytical readiness across&nbsp;Capricor’s&nbsp;therapeutic programs.</span><span data-ccp-props="{}">&nbsp;</span></div>

Quality Control Scientist, Controls

<div>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&nbsp;<strong>Deramiocel&nbsp;</strong>(<em>CAP-1002</em>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div> <div>&nbsp;</div> <div><span style="font-size: 16px;">As a Manufacturing Associate I, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success.</span></div>

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <div> <p><span data-contrast="auto">The Quality Control Associate II, Controls will support the development, qualification, and lifecycle management of analytical control materials used in QC assays. This role will&nbsp;be responsible for&nbsp;generating and&nbsp;maintaining&nbsp;positive and negative controls, performing analytical studies to evaluate assay performance, and supporting troubleshooting and optimization of analytical methods used in QC testing.</span><span data-ccp-props="{}">&nbsp;</span></p> </div> <div> <p><span data-contrast="auto">This position plays&nbsp;an important role&nbsp;in ensuring the reliability and consistency of QC assays by supporting the generation, characterization, and maintenance of assay controls. The individual will work closely with QC scientists and cross-functional teams to support assay performance monitoring and continuous improvement of analytical methods used across&nbsp;Capricor’s&nbsp;therapeutic programs.</span><span data-ccp-props="{}">&nbsp;</span></p> </div> </div>

Quality Control Associate II, Controls

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The Senior Director of Quality provides strategic and operational leadership for all quality activities supporting Capricor’s clinical-stage and advancing commercial-stage organization. This role has full accountability for the design, execution, and continuous improvement of the Quality Management System (QMS) to ensure sustained regulatory compliance, inspection readiness, and robust quality oversight across development, manufacturing (including cell therapy production), and potential commercialization of Deramiocel and StealthX™-based programs.</div> <div>&nbsp;</div> <div>The Senior Director partners closely with executive leadership, Regulatory Affairs, CMC, Clinical, Manufacturing, and other cross-functional teams to enable late-stage development, BLA submissions and responses (including addressing any quality-related aspects of the Deramiocel pathway), commercial readiness, and scalable growth while embedding a proactive, risk-based quality culture across the enterprise.</div>

Senior Director, Quality

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div><span data-contrast="auto">The Director, Quality Assurance &amp; Quality Systems will lead and support quality assurance and quality systems activities for&nbsp;Capricor's&nbsp;clinical and commercial-stage biotechnology operations. The role advances the company's Quality Management System, drives&nbsp;inspection&nbsp;readiness, and ensures quality processes are scalable, compliant, and aligned with late-stage development and commercial launch. The ideal candidate brings hands-on QA and Quality Systems experience, deep knowledge of GMP and FDA requirements, and a proven ability to partner cross-functionally to build a proactive, risk-based quality culture.</span><span data-ccp-props="{&quot;335559739&quot;:240}">&nbsp;</span></div>

Director, Quality Assurance & Quality Systems

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div>

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><p>The Animal Technician will be responsible for performing in vivo studies including compound dosing, sample collection and analysis for data generation. The position will afford the opportunity to work alongside a highly dynamic and collaborative team to develop an entirely new therapeutic modality.</p>

Animal Technician, Preclinical Studies

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div><span data-contrast="auto">In this role, you will oversee the daily operations, maintenance, and repair of pharmaceutical and R&amp;D manufacturing and facility systems, ensuring they&nbsp;operate&nbsp;in a validated state of control. You will manage programs and personnel, drive continuous improvements, and&nbsp;maintain&nbsp;compliance with GMP and regulatory standards while ensuring safe, reliable, and cost-effective facility operations.</span><span data-ccp-props="{}">&nbsp;</span></div>

Facilities Manager

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>As an <strong>MSAT Training Specialist II/III</strong> at Capricor, you will play a pivotal role in ensuring operational excellence and GMP compliance across our cell therapy manufacturing processes. This position focuses on designing and delivering robust training programs, mentoring manufacturing personnel, and maintaining documentation that supports regulatory readiness and high-quality production. Ideal candidates thrive in a dynamic biotech environment, combining technical expertise with a commitment to continuous improvement and team development.</div>

MSAT Training Specialist II/III

<div> <p>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&nbsp;<strong>Deramiocel&nbsp;</strong>(<em>CAP-1002</em>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</p> <p>&nbsp;</p> <div> <p><span style="font-size: 16px;">As a Manufacturing Technician, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trialscommercial production, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success.&nbsp;</span></p> <p>&nbsp;</p> <p><span style="font-size: 16px;">This role is a full time position on our Manufacturing team, this position will be a 2-2-3 work schedule.&nbsp;&nbsp;</span></p> </div> </div>

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <p>The Quality Control Scientist will be a key contributor to Capricor’s mission of delivering innovative cell and regenerative therapies, ensuring the highest standards of product quality at our San Diego facility. This lab-based role is critical in advancing our quality control framework by optimizing and validating analytical methods, facilitating seamless technology transfers, and driving continuous improvement initiatives. The scientist will work closely with cross-functional teams to support the development and commercialization of novel therapies, including cell-based products and exosomes, while ensuring compliance with stringent regulatory standards. This position offers a unique opportunity to shape phase-appropriate QC strategies, implement cutting-edge technologies, and directly impact patient outcomes through robust quality assurance.</p> </div>

Quality Control Scientist

<p>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&nbsp;<strong>Deramiocel&nbsp;</strong>(<em>CAP-1002</em>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</p> <p><span style="font-size: 16px;">As a Manufacturing Associate I, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success.</span></p> <p>&nbsp;</p> <div> <p>This position follows an <strong>AWS/Panama 2-2-3 schedule</strong>, which is a rotating shift pattern designed to provide consistent coverage and extended time off.</p> <p><strong><u>Schedule Details:</u></strong></p> <p><strong style="font-size: 11pt;">12-hour shifts</strong></p> <p><span style="font-size: 11pt;">Week 1: Work </span><strong style="font-size: 11pt;">Monday &amp; Tuesday</strong><span style="font-size: 11pt;">, off </span><strong style="font-size: 11pt;">Wednesday &amp; Thursday</strong><span style="font-size: 11pt;">, work </span><strong style="font-size: 11pt;">Friday–Sunday</strong></p> <p><span style="font-size: 11pt;">Week 2: Off </span><strong style="font-size: 11pt;">Monday &amp; Tuesday</strong><span style="font-size: 11pt;">, work </span><strong style="font-size: 11pt;">Wednesday &amp; Thursday</strong><span style="font-size: 11pt;">, off </span><strong style="font-size: 11pt;">Friday–Sunday</strong></p> <p>&nbsp;</p> <p><span style="font-size: 11pt;">This creates a repeating cycle of </span><strong style="font-size: 11pt;">2 days on, 2 days off, 3 days on</strong><span style="font-size: 11pt;">, then the reverse the following week.</span></p> </div>

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>This position will drive disciplined execution, operational readiness, and process excellence across Capricor’s commercial launch program. This role sits at the center of cross‑functional coordination—ensuring teams are aligned, risks are surfaced early, timelines are maintained, and launch-critical processes are mapped, optimized, and repeatable.</div> <p>The ideal candidate brings experience supporting biotech/pharma commercial launches, paired with strong program management, operational excellence, and process‑improvement capabilities. This role is designed for someone who thrives in structured planning, cross‑functional orchestration, and building scalable frameworks in a fast‑moving, high‑growth environment.</p>

Program Manager, Commercial Operations

Senior Director, Medical Affairs (MD Required)

<div>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&nbsp;<strong>Deramiocel&nbsp;</strong>(<em>CAP-1002</em>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div> <div>&nbsp;</div> <div><span data-contrast="auto">We are seeking an&nbsp;individual&nbsp;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 ideal candidate brings hands-on GMP/GxP auditing experience within the life sciences industry and partners cross-functionally to drive continuous improvement and a strong culture of compliance.</span><span data-ccp-props="{}">&nbsp;</span></div>

Quality Compliance Associate I/II

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><p>We are seeking a detail-oriented Security Analyst to protect our cybersecurity operations within our regulated biotech/pharmaceutical environment. This role combines hands-on security operations with compliance governance, focusing on protecting GMP systems, regulated data, and financially relevant systems in scope for SOX compliance.</p> <p>This is a unique opportunity to work at the intersection of threat operations and regulatory compliance, ensuring adherence to GMP, SOX IT General Controls (ITGCs), and industry security frameworks while actively defending against evolving cyber threats.</p>

Security Analyst

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <div> <p><span data-contrast="auto">The Supplier Quality Specialist/Supervisor is a critical role responsible for overseeing the development and maintenance of a robust supplier quality program, managing external audit programs, and ensuring compliance with Good Manufacturing Practice (GMP) standards. Reporting to Senior Manager Quality Compliance, this position will drive supplier qualifications, conduct risk-based audits, and collaborate with cross-functional teams to maintain high-quality standards and support continuous improvement. The ideal candidate is a detail-oriented professional with extensive experience in supplier quality management and GMP/GLP environments, capable of working independently to meet project goals while ensuring regulatory compliance. This role will play a pivotal part in upholding Capricor’s commitment to quality and excellence in the development of innovative therapies.</span><span data-ccp-props="{}">&nbsp;</span></p> </div> <div> <p><span data-contrast="auto">The team this person will be joining develops and&nbsp;maintains&nbsp;the Supplier Quality Program, conducts supplier qualifications and audits, manages SCAR activities, generates and manages Quality Agreements, and develops SOPs.</span><span data-ccp-props="{}">&nbsp;</span></p> </div> </div>

Supplier Quality Management (SQM) Manager

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>We are seeking a <strong>Scientist</strong> to join our <strong>Pre-Clinical</strong> team to support the progression of our therapeutic programs through the design, execution, and optimization of in vivo research activities and preclinical studies. This role requires deep expertise in in vivo methodologies, strong technical skills, and the ability to perform complex operations in a regulated environment.</div>

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The Medical Science Liaison (MSL) Director is a field-based scientific leader responsible for delivering Capricor's scientific engagement strategy across an assigned territory of national and regional KOLs treating Duchenne muscular dystrophy (DMD) and DMD cardiomyopathy. The role focuses on scientific exchange with thought leaders, treatment centers, and academic institutions in neuromuscular disease, cardiology, and pediatric specialty care; identification of clinical and research opportunities; and translation of field insights into Capricor's medical strategy for Deramiocel. This individual partners closely with the Medical Director, VP Medical Affairs, HEOR / RWE, Pharmacovigilance, Clinical Development, and the broader U.S. MSL team.</div>

Medical Science Liaison (MSL) Director

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <div>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 materials within our facilities. This role requires attention to detail, a commitment to quality, and the ability to work effectively in a fast-paced environment.</div> <div>&nbsp;</div> <div>Operations run between <strong>6:00 AM–6:00 PM</strong>, with roles assigned to one of two set shift windows: <strong>6:00 AM–2:30 PM</strong> or <strong>9:30 AM–6:00 PM</strong>. Openings are distributed across locked weekly schedules—<strong>Sat–Wed, Tue–Sat, Thu–Mon, and Fri–Tue</strong>—and you will be hired into one of these specific schedules. While shifts do not rotate, candidates should maintain flexibility for <strong>1–2 hours of overtime as needed</strong> to support production and shipping demands.</div> </div>

Materials Handler

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>The&nbsp;Process Development&nbsp;Scientist&nbsp;at Capricor&nbsp;will lead&nbsp;development&nbsp;of biomanufacturing&nbsp;processes&nbsp;to&nbsp;enhance&nbsp;product yield, quality, and cost-efficiency&nbsp;with&nbsp;a focus&nbsp;on&nbsp;closed system processes and scale-up.&nbsp;This role is responsible for&nbsp;driving process improvements, evaluatingnew technologies,&nbsp;mentoring&nbsp;junior team members, and collaborating with cross-functional teams to translate discoveries into&nbsp;validated processes.</div>

Process Development Scientist

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <p>The&nbsp;Process Development&nbsp;Scientist&nbsp;at Capricor&nbsp;will lead&nbsp;development&nbsp;of biomanufacturing&nbsp;processes&nbsp;to&nbsp;enhance&nbsp;product yield, quality, and cost-efficiency&nbsp;with&nbsp;a focus&nbsp;on scaling&nbsp;cell therapy manufacturing&nbsp;using&nbsp;a bioreactor.&nbsp;This role is responsible for&nbsp;advancing innovative therapeutic solutions, managing complex projects,&nbsp;helping to mentor&nbsp;junior scientists, and collaborating with cross-functional teams to translate discoveries into&nbsp;validated processes.</p> </div>

Process Development Scientist - Bioreactor

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div><span style="font-size: 11pt;">The Data Science &amp; Solutions team is seeking a junior data analytics professional to support research, manufacturing, and analytical data initiatives in a biotechnology environment.</span></div>

Data Analytics Associate

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div> <div>We are looking for an exceptional individual to join our growing team as a Warehouse Lead. The Warehouse Lead will play a critical role in supporting our manufacturing and logistics operations by managing inventory, processing shipments, and ensuring the efficient movement of materials within our facilities. This role requires attention to detail, a commitment to quality, and the ability to work effectively in a fast-paced environment.</div> <div>&nbsp;</div> <div>Operations run between <strong>6:00 AM–6:00 PM</strong>, with roles assigned to one of two set shift windows: <strong>6:00 AM–2:30 PM</strong> or <strong>9:30 AM–6:00 PM</strong>. Openings are distributed across locked weekly schedules—<strong>Sat–Wed, Tue–Sat, Thu–Mon, and Fri–Tue</strong>—and you will be hired into one of these specific schedules. While shifts do not rotate, candidates should maintain flexibility for <strong>1–2 hours of overtime as needed</strong> to support production and shipping demands.</div> </div>

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>
<p>The Operations Coordinator is responsible for maintaining the day-to-day functionality, safety, and professionalism of the workplace. This role ensures the office, lab-adjacent spaces, and common areas remain organized, clean, and compliant with company policies. &nbsp;</p>
<p>This individual will regularly walk the facility floors to monitor workplace conditions, support employees and visitors, and coordinate with facilities, security, and vendors to resolve issues quickly. In a small biotech environment, this role is highly visible and critical to maintaining a productive, safe, and welcoming workplace.&nbsp;</p>
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<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div><span data-teams="true">This is an overnight (graveyard) shift role supporting off-hours GMP manufacturing. </span>As a Quality Assurance Specialist at Capricor, you will serve as the primary Quality representative during overnight manufacturing operations (Graveyard Shift). In this role, you will provide Quality Assurance oversight for manufacturing, cryopreservation, and support activities while ensuring compliance with cGMP regulations, internal procedures, and quality standards. The ideal candidate brings experience in GMP-regulated environments, strong attention to detail, and the ability to make sound quality decisions independently during off-shift operations.&nbsp;</div>

Quality Assurance Specialist - Night Shift

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>
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<p><strong><span data-contrast="auto">Position Summary</span><span data-ccp-props="{}">&nbsp;</span></strong></p>
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<p><span data-contrast="auto">The Quality Control Associate, Raw&nbsp;Materials&nbsp;is responsible for performing routine testing and documentation of raw materials used in&nbsp;Capricor’s&nbsp;manufacturing processes. This role ensures all incoming materials meet established specifications, regulatory requirements, and GMP standards.</span><span data-ccp-props="{}">&nbsp;</span></p>
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<p><span data-contrast="auto">As part of the QC Raw Materials team, you will perform hands</span>‑<span data-contrast="auto">on laboratory work, maintain accurate and compliant documentation, support investigations, and collaborate with QC, QA, Procurement, and Manufacturing teams to ensure timely material readiness. This is a new headcount created to support the expansion of&nbsp;Capricor’s&nbsp;manufacturing and quality operations.</span><span data-ccp-props="{}">&nbsp;</span></p>
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<p><span data-ccp-props="{}">&nbsp;</span><strong><span data-contrast="auto">Team Mission</span><span data-ccp-props="{}">&nbsp;</span></strong></p>
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<p><span data-contrast="auto">The QC Raw Materials team ensures that all raw materials used in manufacturing consistently meet quality, safety, and regulatory standards. By verifying material identity, quality, and compliance, the team enables reliable production and supports&nbsp;Capricor’s&nbsp;broader mission of delivering high</span>‑<span data-contrast="auto">quality therapeutic products.</span><span data-ccp-props="{}">&nbsp;</span></p>
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<p><span data-ccp-props="{}">&nbsp;</span><span data-contrast="auto">Responsibilities</span><span data-ccp-props="{}">&nbsp;</span></p>
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<ul role="list" style="list-style-type: disc;">
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="51" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1" role="listitem">
<p><span data-contrast="auto">Perform routine quality control testing of raw materials in accordance with approved specifications and SOPs.</span><span data-ccp-props="{}">&nbsp;</span></p>
</li>
</ul>
</div>
<div>
<ul role="list" style="list-style-type: disc;">
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="51" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="2" data-aria-level="1" role="listitem">
<p><span data-contrast="auto">Prepare samples, reagents, standards, and required materials for testing.</span><span data-ccp-props="{}">&nbsp;</span></p>
</li>
</ul>
</div>
<div>
<ul role="list" style="list-style-type: disc;">
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="51" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="3" data-aria-level="1" role="listitem">
<p><span data-contrast="auto">Accurately document all test results in laboratory notebooks, forms, and electronic systems following GMP and data integrity standards.</span><span data-ccp-props="{}">&nbsp;</span></p>
</li>
</ul>
</div>
<div>
<ul role="list" style="list-style-type: disc;">
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="51" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="4" data-aria-level="1" role="listitem">
<p><span data-contrast="auto">Identify, document, and report any out</span>‑<span data-contrast="auto">of</span>‑<span data-contrast="auto">specification (OOS), atypical, or questionable results to senior QC personnel.</span><span data-ccp-props="{}">&nbsp;</span></p>
</li>
</ul>
</div>
<div>
<ul role="list" style="list-style-type: disc;">
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="51" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="5" data-aria-level="1" role="listitem">
<p><span data-contrast="auto">Support investigations, deviations, and CAPA activities as assigned.</span><span data-ccp-props="{}">&nbsp;</span></p>
</li>
</ul>
</div>
<div>
<ul role="list" style="list-style-type: disc;">
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="51" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="6" data-aria-level="1" role="listitem">
<p><span data-contrast="auto">Maintain laboratory organization, cleanliness, and adherence to safety and GMP practices.</span><span data-ccp-props="{}">&nbsp;</span></p>
</li>
</ul>
</div>
<div>
<ul role="list" style="list-style-type: disc;">
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="51" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="7" data-aria-level="1" role="listitem">
<p><span data-contrast="auto">Assist with equipment operation, calibration, routine checks, and maintenance.</span><span data-ccp-props="{}">&nbsp;</span></p>
</li>
</ul>
</div>
<div>
<ul role="list" style="list-style-type: disc;">
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="51" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="8" data-aria-level="1" role="listitem">
<p><span data-contrast="auto">Follow all GMP, safety, and compliance procedures consistently.</span><span data-ccp-props="{}">&nbsp;</span></p>
</li>
</ul>
</div>
<div>
<ul role="list" style="list-style-type: disc;">
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="51" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="9" data-aria-level="1" role="listitem">
<p><span data-contrast="auto">Collaborate with QC, QA, Manufacturing, and Supply Chain groups to ensure timely material testing and release.</span><span data-ccp-props="{}">&nbsp;</span></p>
</li>
</ul>
</div>
</div>
<div>
<div>
<ul role="list" style="list-style-type: disc;">
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="51" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="10" data-aria-level="1" role="listitem">
<p><span data-contrast="auto">Participate in training, audits, and ongoing process improvement initiatives.</span><span data-ccp-props="{}">&nbsp;</span></p>
</li>
</ul>
</div>
</div>
</div>

Quality Control Associate, Raw Materials

<div>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&nbsp;<b>Deramiocel&nbsp;</b>(<i>CAP-1002</i>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>
<p style="text-align: justify; margin: 0in; font-size: 11pt; font-family: 'Times New Roman', serif;"><span style="font-family: 'Times New Roman', serif;">Capricor is seeking a self-motivated team player with attention to detail, who enjoys organizing, making processes better, and making a difference in patient lives.&nbsp; </span><span style="font-family: 'Times New Roman', serif;">The Quality Assurance QA Associate II – Quality Events Team (QET) is responsible for cross-functional triage of issues and managing, investigating, and resolving deviations, non-conformances, and corrective and preventive actions (CAPAs) in compliance with cGMP, SOPs, and regulatory requirements. This role ensures the consistent application of quality standards across manufacturing, laboratory, and clinical operations while supporting continuous improvement initiatives.</span></p>
<p style="margin: 0in -1.5pt 0in 0in; text-align: justify; font-size: 11pt; font-family: Calibri, sans-serif;">&nbsp;</p>
<span style="font-size: 11.0pt; font-family: 'Times New Roman', serif;">The position will be hybrid, Thursday-Monday, 8am-5pm. &nbsp;&nbsp;</span></div>

<div>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&nbsp;<strong>Deramiocel&nbsp;</strong>(<em>CAP-1002</em>), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome 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.</div><div><br></div><div>
<div>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 materials within our facilities. This role requires attention to detail, a commitment to quality, and the ability to work effectively in a fast-paced environment.</div>
<div>&nbsp;</div>
<div>Operations run between <strong>6:00 AM–6:00 PM</strong>, with roles assigned to one of two set shift windows: <strong>6:00 AM–2:30 PM</strong> or <strong>9:30 AM–6:00 PM</strong>. Openings are distributed across locked weekly schedules—<strong>Sat–Wed, Tue–Sat, Thu–Mon, and Fri–Tue</strong>—and you will be hired into one of these specific schedules. While shifts do not rotate, candidates should maintain flexibility for <strong>1–2 hours of overtime as needed</strong> to support production and shipping demands.</div>
</div>

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