GLP QA Specialist II: Quality Systems & Documentation
Celldex
Celldex is seeking a QA professional to maintain GLP document control, manage lab notebooks, and oversee GLP QA periodic reports. The role supports GLP testing, trends GLP QA information, and conducts internal GLP audits, ensuring cGMP compliance. A BS/BA in Life Sciences and 1–3 years of QA experience in biotech/pharma are preferred, with strong EDMS and MS Office skills. The position offers base compensation with a comprehensive benefits package, including discretionary bonuses and health #J-18808-Ljbffr Celldex
Vacancy posted 3 days ago
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