Senior QA Specialist, GMP & Documentation Lead
Listed on 2026-09-22
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
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
We would love to welcome a new Senior QA Specialist, GMP & Documentation Lead to our organisation in NC, United States.
As a Senior QA Specialist, GMP & Documentation Lead, you will play an important part at Initial Therapeutics, Inc. in NC, United States.
We invite applications for the Senior QA Specialist, GMP & Documentation Lead position located in NC, United States.
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