Capricor Therapeutics, Inc.
Quality Assurance Associate I
Capricor Therapeutics, Inc., San Diego, California, United States, 92189
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. We are seeking a self‑motivated team player with attention to detail, who enjoys organizing, making processes better, and making a difference in patient lives. The successful candidate will serve an essential role in supporting clinical product launch and production. This includes batch record review, review of raw materials, deviation investigation, label issuance, and word processing, tracking, issuing, distributing, and archiving company‑wide GLP/GCP/GMP controlled documentation, training, and facility support systems. This role is located at Capricor’s headquarters in San Diego, CA. Responsibilities
Support clinical product manufacturing by batch record review, label printing, product packaging, and shipping Conduct or coordinate deviation investigations, corrective and preventative actions (CAPA), change controls, company‑wide training, and internal audits. Write associated reports Process controlled documentation through the GxP (GLP/GCP/GMP) documentation system, including but not limited to word processing, tracking, issuing, distributing, and archiving, utilizing manual or an electronic document management system Coordinate / track / archive: controlled records (i.e., batch/test records, logbooks, validation documents, labels, reports, forms, etc.) for change controls, deviations, CAPAs, audits, training, equipment calibration and preventative maintenance Write and/or review policies, standards, procedures and work instructions to document quality documentation processes and practices Support supplier and material management, including ordering, incoming receipt, and record keeping Perform review and release of incoming materials Inventory database management including accurate and timely updating of lot numbers and quantities Collaborate on development / improvement and implementation of material, facility and quality management systems Other required duties as may be assigned Requirements
Bachelor’s Degree and 2+ years of experience in a cGMP environment Knowledge of standard processes involved in document control and experience in an FDA regulated environment Experience in Aseptic Processing a plus Precise attention to detail Excellent record‑keeping skills Strong, demonstrable computer skills in MS Word, Excel, Visio, Access, Adobe suite, and database systems Familiar with Quality Systems and records management in a cGMP environment Strong communication and problem‑solving skills Results oriented with dedication to compliance and customer service Strong initiative and follow‑through Comfortable working in a fast‑paced and dynamic environment Ability to gown and work in a classified area as required Work Environment / Physical Demands
Must be able to sit and stand for extended periods Must be able to lift/carry reports and materials up to 40 pounds, move about the office, communicate efficiently and effectively on the telephone or in person, and complete required paperwork $65,000 - $75,000 a year Comprehensive benefits package, including health insurance, retirement plans, and opportunities for professional development. Why Capricor?
Capricor Therapeutics is an industry leader in cell and exosome therapy, pushing boundaries to create innovative treatments that raise the standard of care. Grounded in integrity and driven by science, our team is committed to making a meaningful impact through patient‑centered innovation. Join us and be part of a team that’s changing lives—help us shape the future of healthcare. Come work with us!
At Capricor, we offer a collaborative work environment that supports your professional growth. Join a passionate team committed to transforming the lives of patients and pushing the boundaries of medical science Why Capricor?
Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient‑centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission‑driven group that’s transforming lives with every breakthrough. Come Work With Us!
At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting‑edge therapies. Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.
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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. We are seeking a self‑motivated team player with attention to detail, who enjoys organizing, making processes better, and making a difference in patient lives. The successful candidate will serve an essential role in supporting clinical product launch and production. This includes batch record review, review of raw materials, deviation investigation, label issuance, and word processing, tracking, issuing, distributing, and archiving company‑wide GLP/GCP/GMP controlled documentation, training, and facility support systems. This role is located at Capricor’s headquarters in San Diego, CA. Responsibilities
Support clinical product manufacturing by batch record review, label printing, product packaging, and shipping Conduct or coordinate deviation investigations, corrective and preventative actions (CAPA), change controls, company‑wide training, and internal audits. Write associated reports Process controlled documentation through the GxP (GLP/GCP/GMP) documentation system, including but not limited to word processing, tracking, issuing, distributing, and archiving, utilizing manual or an electronic document management system Coordinate / track / archive: controlled records (i.e., batch/test records, logbooks, validation documents, labels, reports, forms, etc.) for change controls, deviations, CAPAs, audits, training, equipment calibration and preventative maintenance Write and/or review policies, standards, procedures and work instructions to document quality documentation processes and practices Support supplier and material management, including ordering, incoming receipt, and record keeping Perform review and release of incoming materials Inventory database management including accurate and timely updating of lot numbers and quantities Collaborate on development / improvement and implementation of material, facility and quality management systems Other required duties as may be assigned Requirements
Bachelor’s Degree and 2+ years of experience in a cGMP environment Knowledge of standard processes involved in document control and experience in an FDA regulated environment Experience in Aseptic Processing a plus Precise attention to detail Excellent record‑keeping skills Strong, demonstrable computer skills in MS Word, Excel, Visio, Access, Adobe suite, and database systems Familiar with Quality Systems and records management in a cGMP environment Strong communication and problem‑solving skills Results oriented with dedication to compliance and customer service Strong initiative and follow‑through Comfortable working in a fast‑paced and dynamic environment Ability to gown and work in a classified area as required Work Environment / Physical Demands
Must be able to sit and stand for extended periods Must be able to lift/carry reports and materials up to 40 pounds, move about the office, communicate efficiently and effectively on the telephone or in person, and complete required paperwork $65,000 - $75,000 a year Comprehensive benefits package, including health insurance, retirement plans, and opportunities for professional development. Why Capricor?
Capricor Therapeutics is an industry leader in cell and exosome therapy, pushing boundaries to create innovative treatments that raise the standard of care. Grounded in integrity and driven by science, our team is committed to making a meaningful impact through patient‑centered innovation. Join us and be part of a team that’s changing lives—help us shape the future of healthcare. Come work with us!
At Capricor, we offer a collaborative work environment that supports your professional growth. Join a passionate team committed to transforming the lives of patients and pushing the boundaries of medical science Why Capricor?
Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient‑centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission‑driven group that’s transforming lives with every breakthrough. Come Work With Us!
At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting‑edge therapies. Please note that Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Additionally, Capricor will never ask potential employees to send a check or money to the Company for any reason.
#J-18808-Ljbffr