Quality Assurance Associate II/III

Capricor Therapeutics is a biotechnology company seeking a Quality Assurance Associate III to join their team. The role involves leading batch record review, deviation investigations, and management of controlled documentation across GLP/GCP/GMP systems.

Requirements

• Bachelor’s degree in a scientific discipline (Life Sciences, Engineering, or related field)
• 3–5 years of progressive QA experience in a cGMP-regulated environment
• Demonstrated expertise in batch record disposition, deviation/CAPA management, and change control oversight
• Strong knowledge of FDA regulations (21 CFR Parts 210/211), ICH guidelines, and quality systems
• Ability to author and approve SOPs and quality documentation; experience with electronic document management systems
• Excellent communication, problem-solving, and decision-making skills
• Proven ability to work independently, lead initiatives, and mentor junior staff

Benefits

• $70,000 - $92,500 a year