GMP Documentation & QA Compliance Associate II
Celldex
Celldex Therapeutics, Inc. in Fall River, MA seeks a Quality Assurance Associate II to manage GMP documentation with EDMS workflows, format and issue records, and support material release. You’ll maintain labeling, SOPs, and training files while assisting with audits and off-site storage logistics. The role requires GMP experience, strong organization, and proficiency with MS Office and EDMS in a fast-paced QA environment. #J-18808-Ljbffr Celldex
Vacancy posted 3 days ago
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