Quality Systems Associate 2
Capricor Therapeutics(1 month ago)
About this role
The Quality Systems Associate at Capricor Therapeutics supports and maintains the company’s Quality Management System to ensure compliance with FDA, GMP, ISO 9001, and internal standards. The role is primarily office-based and focuses on documentation, system administration, and quality records management. The position operates in a fast-paced biotech environment and involves regular interaction with QA, QC, Manufacturing, Facilities, and R&D teams. It offers growth opportunities for individuals looking to build a career in quality within a regulated biotechnology setting.
Required Skills
- Quality Management
- Document Control
- CAPA Management
- Internal Audits
- External Audits
- Training Coordination
- Deviation Management
- Nonconformance Management
- Change Control
- Cross-Functional Collaboration
+12 more
Qualifications
- Bachelor’s Degree in Life Sciences
- Bachelor’s Degree in Engineering
About Capricor Therapeutics
capricor.comCapricor 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.
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