Post-Marketing Quality Compliance Associate 2

Capricor Therapeutics(1 month ago)

San Diego, CAOnsiteFull TimeMedior$99,506 - $132,688 (estimated)Quality Compliance

About this role

This Quality Compliance role at Capricor Therapeutics is responsible for auditing biopharma operations to ensure adherence to regulatory requirements and internal procedures. The position supports both internal and supplier audits, inspection readiness, and continuous improvement of quality systems. It sits within a mission-driven biotechnology company focused on cell and exosome-based therapies for rare diseases. The role is based onsite in San Diego and interacts broadly with functions such as QA/QC, Manufacturing, Regulatory, and Supply Chain.

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Required Skills

GxP Auditing
Internal Audits
Supplier Audits
Risk-Based Auditing
Audit Reporting
CAPA Management
Inspection Readiness
Gap Assessment
Cross-Functional Collaboration
Quality Systems

+10 more

Qualifications

BS in Chemistry
BS in Biology
BS in Engineering
Certified Quality Auditor

About Capricor Therapeutics

capricor.com

Capricor Therapeutics, Inc. (NASDAQ: CAPR) is a San Diego–based biotechnology company developing cell- and exosome-based therapeutics for muscular and other select diseases. Its lead candidate, deramiocel (CAP‑1002), is an allogeneic cell therapy currently in Phase 3 clinical development for Duchenne muscular dystrophy. Capricor is also advancing exosome technology as a next‑generation platform, engineering exosomes to deliver nucleic acids and proteins to treat or prevent a variety of diseases. The company focuses on translating these platforms into novel therapeutic and preventive products.