Clinical Labeling QA Specialist - Start-Up & Compliance
Listed on 2026-09-18
-
Quality Assurance - QA/QC
Data Analyst -
Healthcare
Data Scientist
Kriya Therapeutics, Inc. is seeking a Quality Assurance Specialist in RTP, NC to review clinical labeling and batch records, and support site start-up activities. The role ensures cGMP compliance and provides QA input to manufacturing and regulatory teams.
The candidate will review deviations, CAPAs, change controls, and SOPs, while supporting electronic batch records and on-floor quality during manufacturing transitions. A 2+ year QA background in biologics/pharma is needed.
We would love to welcome a new Clinical Labeling QA Specialist
- Start-Up & Compliance to our team in NC, United States.
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 Clinical Labeling QA Specialist
- Start-Up & Compliance role in the description above.
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