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
#J-18808-LjbffrGMP Data Integrity & Validation Specialist in madison at Unknown Company
This position is listed as full time and onsite.