Quality Assurance Associate II Clinical GMP Compliance
Capricor Therapeutics, Inc.
Capricor Therapeutics is seeking a Quality Assurance Associate II to support batch record review, deviations, and controlled documentation in a cGMP environment. The role involves document control, training records, and collaboration with the QA team to ensure regulatory readiness. The ideal candidate has a biology/biotech background and up to 3 years of regulated industry experience, with strong attention to detail and communication skills. #J-18808-Ljbffr Capricor Therapeutics, Inc.
Vacancy posted 2 days ago
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