Senior QA Specialist, GMP & Documentation Lead
Initial Therapeutics, Inc.
Protara Therapeutics seeks a Senior Quality Specialist to provide QA support for GMP activities, reviewing controlled documents and records for accuracy, completeness, and compliance. You will identify gaps, advise cross-functional partners, and help strengthen the Quality Management System and inspection readiness. This role requires on-site work five days per week and involves collaboration with QA, Manufacturing, and Regulatory teams to ensure product quality and patient safety across #J-18808-Ljbffr Initial Therapeutics, Inc.
Vacancy posted 2 days ago
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