Senior QA Specialist — GMP Documentation & Compliance
Listed on 2026-09-22
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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.
This is a genuine opening to take on the Senior QA Specialist — GMP Documentation & Compliance role at Protara Therapeutics, Inc.
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 & Compliance role in the description above.
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