About this role
Quality Compliance Associate I/II at Capricor Therapeutics. Location: San Diego, California, United States. Role: planning audits, documenting findings, tracking CAPAs Requirements: Bachelor's in a scientific/technical field or equivalent; 1–2 years auditing experience in regulated biopharma/medical device industries; knowledge of FDA 21 CFR, ICH Q, EU GMP; audit, CAPA, and technical writing skills. Category: Legal and Compliance Seniority: Entry Level Certifications: cqa Commitment: Full Time Workplace: Onsite Languages: English