GMP Deviation Investigator & CAPA Writer
Process Alliance
Process Alliance is hiring a Deviation Writer to join our pharmaceutical manufacturing team in Indianapolis, Indiana. This full-time, on-site role focuses on documenting and investigating GMP deviation investigations and supporting CAPA activities. The ideal candidate has a bachelor’s degree in a scientific or engineering field, 1–2+ years in pharma, and strong writing and analytical skills. Packaging and QC lab experience are a plus; authorization to work in the U.S. is required. #J-18808-Ljbffr Process Alliance
Vacancy posted 4 days ago
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