GMP Data Integrity & Validation Specialist
Listed on 2026-10-07
-
Quality Assurance - QA/QC
Data Analyst, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
United Pharma is seeking an experienced CSV & Data Integrity Specialist to support a GMP remediation project in Madison, WI. This onsite consultant role focuses on remediating Data Integrity gaps across Rockwell/Allen‑Bradley PLC‑based systems, developing and updating validation protocols, executing testing, and documenting results for Quality approval.
The ideal candidate has 4–7 years of experience in CSV/Data Integrity within GMP environments, strong knowledge of 21 CFR Part 11 and related
We are currently recruiting a GMP Data Integrity & Validation Specialist for our team in Madison, WI, 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 GMP Data Integrity & Validation Specialist role in the description above.
We appreciate your interest in this position.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).