A growing pharmaceutical company in Fairfield, NJ is seeking a detail-oriented QA Associate to support daily Quality Assurance operations. The ideal candidate should have at least 1 year of experience in a regulated cGMP environment, strong documentation skills, and the ability to multitask. Responsibilities include managing batch records, preparing documentation, and supporting audits. Join a collaborative team committed to quality and continuous improvement.
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...Open-Source Intelligence (OSINT) Analyst - Team Lead Xcelerate Solutions is seeking an OSINT Analyst Lead assessing contractor compliance with the physical security requirements of sensitive Arms, Ammunition, and Explosives (AA&E) contractors who manufacture, test,...
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