Capricor Therapeutics

Quality Control Associate, Raw Materials

San Diego, CA

Sponsorship not specified$70k-$87kDetected 36 days ago

ExpressSupply ChainProcess ImprovementProcurementRecruitingClinical Laboratory TechniquesGMPCommunicationCollaborationMicrosoft Office

About the role

The Quality Control Associate, Raw Materials is responsible for performing routine testing and documentation of raw materials used in Capricor's manufacturing processes.
The QC Raw Materials team ensures that all raw materials used in manufacturing consistently meet quality, safety, and regulatory standards.

Perform routine quality control testing of raw materials in accordance with approved specifications and SOPs.
Accurately document all test results in laboratory notebooks, forms, and electronic systems following GMP and data integrity standards.
Identify, document, and report any out ‑ of ‑ specification (OOS), atypical, or questionable results to senior QC personnel.
Support investigations, deviations, and CAPA activities as assigned.
Maintain laboratory organization, cleanliness, and adherence to safety and GMP practices.
Collaborate with QC, QA, Manufacturing, and Supply Chain groups to ensure timely material testing and release.
At the forefront of our innovation is Deramiocel ( CAP-1002 ), our lead cell therapy in late-stage development for Duchenne muscular dystrophy.

Bachelor's degree in Life Sciences, Chemistry, Biotechnology, or a related discipline.
Associate II: 1+ years of QC experience in a regulated environment (pharma, biotech, or manufacturing).
Strong attention to detail and ability to follow SOPs and regulated procedures.
Strong documentation skills and the ability to work efficiently with multiple samples and priorities.
Familiarity with GMP or regulated laboratory environments.
1+ years of QC experience in a regulated environment (pharma, biotech, or manufacturing).
Prepare samples, reagents, standards, and required materials for testing.

Working knowledge of GMP, quality systems, and raw materials workflows.
Experience with analytical techniques such as FTIR, endotoxin testing, wet chemistry, or similar raw material identification methods.
Experience with laboratory data systems (LIMS) and Microsoft Office programs.
Strong communication skills and ability to work effectively in a team environment.
Work Environment & Physical Demands
Laboratory ‑ based role with regular work in GMP areas.
Prolonged periods of computer use for documentation, analysis, and reporting.
Occasional lifting of materials or equipment up to 20 pounds.

We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology.

This listing is sourced directly from Capricor Therapeutics's careers page and normalized into a canonical job model.