Senior QA Specialist — GMP Documentation & Compliance
Listed on 2026-09-30
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager -
Pharmaceutical
Regulatory Compliance Specialist
Protara Therapeutics, Inc. seeks a Senior Quality Specialist to provide QA support for GMP activities, review controlled documents, and help strengthen the Quality Management System. On-site 5 days/week, you will work with cross-functional teams to close gaps and improve data integrity.
Ideal candidates have 5+ years in GMP QA, experience with batch release, CAPAs, and CMOs, plus a strong attention to detail and clear communication.
We are seeking a motivated Senior QA Specialist — GMP Documentation & Compliance to join Protara Therapeutics, Inc. in NC, United States.
Learn more about the Senior QA Specialist — GMP Documentation & Compliance role in the description above.
We appreciate your interest in this position.
Join Protara Therapeutics, Inc. and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
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