Senior QA Specialist II - Batch Disposition & GMP Compliance

A pharmaceutical company in North Carolina is seeking a Senior Quality Specialist II to manage GMP compliance and Quality Assurance activities. The role requires strong knowledge of cGMPs and FDA regulations, alongside at least 8 years of relevant experience. The successful candidate will handle batch documentation, approve investigations, and conduct audits, ensuring product quality in line with industry standards. Excellent organizational and software skills are essential for managing multiple tasks effectively.
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