QA Associate II - Drive cGMP in Clinical Manufacturing
Capricor Therapeutics, Inc.
Capricor Therapeutics, Inc. is seeking a Quality Assurance Associate II to ensure compliance with cGMP and regulatory standards. This role involves assisting in batch record review, managing documentation, and supporting quality management systems. The ideal candidate will have a Bachelor’s in a relevant field and 0–3 years of experience in a regulated environment. Strong attention to detail and organizational skills are essential. The position is based in Emeryville, California. #J-18808-Ljbffr Capricor Therapeutics, Inc.
Vacancy posted 3 days ago
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