Senior QA Specialist, Biotech (cGMP & Regulatory)
Cellphire Therapeutics, Inc.
Cellphire Therapeutics, Inc. in Rockville, Maryland, is seeking a QA Associate III to ensure cGMP compliance, regulatory alignment, and robust quality systems. The role collaborates with Manufacturing, QC, and Regulatory teams to maintain product quality in a fast-paced biotech setting. The ideal candidate has at least 5 years of QA experience, familiarity with FDA regulations, and hands-on quality system improvement. The position offers competitive pay and comprehensive benefits. #J-18808-Ljbffr Cellphire Therapeutics, Inc.
Vacancy posted 10 hours ago
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