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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.... Upbeat individuals interested in staying active & fit while earning above-average income are perfect for this role. Earn $20.00 per hour while in training Full time second shift ONLY Perishable (Refrigerated)- about 28- 60 7:00 pm until the work is completed...