Senior QA Specialist, GMP & Documentation Lead
Listed on 2026-09-30
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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
Step into the Senior QA Specialist, GMP & Documentation Lead role at Initial Therapeutics, Inc. in NC, United States and grow with us.
The advertised compensation is 80.000 - 86.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior QA Specialist, GMP & Documentation Lead role in the description above.
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