SupportFinity™
Quality Control Analytical Scientist
SupportFinity™, 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.
The
Quality Control Analytical 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.
Responsibilities
Optimize and troubleshoot QC methods to enhance performance, consistency, and efficiency
Support method qualification, validation, and lifecycle management per regulatory expectations (ICH, USP, FDA)
Perform data trending and analysis to monitor assay performance and detect method variability or drift
Collaborate with Analytical Development for seamless method transfers and onboarding of new assays into the QC laboratory
Draft and review method SOPs, validation protocols/reports, and technical documentation
Contribute to investigations, CAPAs, and continuous improvement initiatives within the QC function
Evaluate and implement new technologies or instrumentation to improve assay robustness and throughput
Provide technical documentation and SME input for regulatory inspections and audits
Participate in risk assessments, gap analyses, and change control activities related to QC methods
Train QC analysts on new or optimized assays to ensure consistent and compliant execution
Author and review technical reports, method development summaries, and QC method lifecycle documents
Maintain GMP documentation and laboratory practices with a strong lab‑based presence
Requirements
Ph.D. in a relevant Biological Science discipline
2–5 years of experience in a GMP Quality Control laboratory or GMP/GLP setting
Hands‑on experience with laboratory methods including flow cytometry, Real‑Time PCR, DNA isolation, ELISA, bioactivity assays, and next‑generation sequencing
Knowledge of FDA regulations, ICH guidelines, USP standards, and cGMP requirements for cell therapy or biologics
Proven expertise in method qualification and validation
Ability to independently perform laboratory analysis, troubleshoot, and improve methods
Demonstrated history of successful, independent laboratory work
Excellent communication skills and ability to collaborate effectively in a team environment
Work Environment / Physical Demands
Must be able to sit or stand for extended periods, move around the facility, communicate effectively, and lift/carry up to 40 lbs
Ability to gown and work in a classified area as required
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.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
This role offers a competitive salary based on experience and qualifications. Additional benefits include health/dental/vision insurance, paid time off, parental leave, 401(k) retirement plan, company stock options, and bonus eligibility.
About the company
Capricor Therapeutics, Inc.
#J-18808-Ljbffr
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.
The
Quality Control Analytical 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.
Responsibilities
Optimize and troubleshoot QC methods to enhance performance, consistency, and efficiency
Support method qualification, validation, and lifecycle management per regulatory expectations (ICH, USP, FDA)
Perform data trending and analysis to monitor assay performance and detect method variability or drift
Collaborate with Analytical Development for seamless method transfers and onboarding of new assays into the QC laboratory
Draft and review method SOPs, validation protocols/reports, and technical documentation
Contribute to investigations, CAPAs, and continuous improvement initiatives within the QC function
Evaluate and implement new technologies or instrumentation to improve assay robustness and throughput
Provide technical documentation and SME input for regulatory inspections and audits
Participate in risk assessments, gap analyses, and change control activities related to QC methods
Train QC analysts on new or optimized assays to ensure consistent and compliant execution
Author and review technical reports, method development summaries, and QC method lifecycle documents
Maintain GMP documentation and laboratory practices with a strong lab‑based presence
Requirements
Ph.D. in a relevant Biological Science discipline
2–5 years of experience in a GMP Quality Control laboratory or GMP/GLP setting
Hands‑on experience with laboratory methods including flow cytometry, Real‑Time PCR, DNA isolation, ELISA, bioactivity assays, and next‑generation sequencing
Knowledge of FDA regulations, ICH guidelines, USP standards, and cGMP requirements for cell therapy or biologics
Proven expertise in method qualification and validation
Ability to independently perform laboratory analysis, troubleshoot, and improve methods
Demonstrated history of successful, independent laboratory work
Excellent communication skills and ability to collaborate effectively in a team environment
Work Environment / Physical Demands
Must be able to sit or stand for extended periods, move around the facility, communicate effectively, and lift/carry up to 40 lbs
Ability to gown and work in a classified area as required
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.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
This role offers a competitive salary based on experience and qualifications. Additional benefits include health/dental/vision insurance, paid time off, parental leave, 401(k) retirement plan, company stock options, and bonus eligibility.
About the company
Capricor Therapeutics, Inc.
#J-18808-Ljbffr