Pharmaceutical Quality Assurance Lead — 3rd Shift (GMP)
The International Society for Pharmaceutical Engineering, Inc.
The International Society for Pharmaceutical Engineering, Inc. is seeking a Quality Assurance professional for a 3rd shift in a FDA-regulated manufacturing environment in Rock Hill, SC. The role involves training staff, ensuring GMP compliance, and reviewing batch records and SOPs to maintain quality throughout production. Responsibilities include supervising quality control personnel, performing inspections, maintaining calibration of equipment, and supporting audits. #J-18808-Ljbffr The International Society for Pharmaceutical Engineering, Inc.
Vacancy posted 1 day ago
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