Posted:
June 15, 2026
Location:
Melville, NY, United States

Job Description

Kedrion Biopharma Inc. is an international company that collects and fractionates blood plasma to produce and distribute plasma-derived therapeutic products for us in treating and preventing serious diseases, disorders and conditions such as Hemophilia, Primary Immune System Deficiencies and Rh-Sensitization.

**Job Summary**

Be the frontline guardian of quality and compliance on the manufacturing floor. As a Good Documentation Practices (GDP) Monitor, you will play a critical real-time role ensuring data integrity, regulatory compliance, and high-quality documentation. Partnering closely with Manufacturing and Operations teams, you will help identify and correct documentation issues as they happen—preventing errors before they impact product quality or release timelines while promoting a culture of accuracy and accountability.

**What you'll do**

+ Perform real-time reviews of batch records, logbooks, cleaning logs, and production documentation to ens...

Apply for this Job

Submit your application for the Good Documentation Practice Monitor DAYS 6AM-4PM CONTRACT POSITION position at Kedrion Biopharma.

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Job Overview

Job Type: Full-time
Location: Melville, United States
Posted: June 15, 2026
Deadline: June 20, 2026