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Lead Validation Specialist, Pharmaceutical Manufacturing
hace 1 mes
We are seeking an experienced Lead Validation Specialist to support our pharmaceutical manufacturing process validation protocols development execution and reporting in Manati, PR.
The successful candidate will have a strong background in process validation within the FDA regulated industry and excellent communication skills both verbal and written. Additionally, they will possess thorough knowledge of GMP regulations and guidelines, as well as experience with risk analysis and risk management practices and tools.
