GLP QA Specialist II - Elevate Quality Systems & Compliance
Celldex Therapeutics, Inc.
Celldex Therapeutics, Inc. is seeking a QA professional to maintain GLP document control, manage lab notebooks, and support QA systems. The role emphasizes accuracy, independence, and cross-functional collaboration to uphold FDA GLP compliance. Responsibilities include periodic reports, internal audits, and timely dissemination of quality documents. Strong communication and teamwork are essential for success in a fast-paced biotech environment. #J-18808-Ljbffr Celldex Therapeutics, Inc.
Vacancy posted 3 days ago
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