Why This Role Stands Out
This on-site Validation Specialist role offers a fantastic opportunity to contribute to a reputable company while gaining hands-on experience in a GMP environment, developing critical validation skills. If you're a detail-oriented professional with pharmaceutical validation experience and a knack for cross-functional collaboration, you'll thrive here and find a rewarding challenge. Apply today to explore this exciting contract position!
Quick Overview
Job Description
Job Description -
QA Validation Specialist
Location: Wilson, NC 27893 (4700 International Blvd. West, Wilson, NC) ?? Onsite: Local Candidates Only (Commute Not to Exceed 60 Miles/60 Minutes)
Nearby ZIP Codes: 27893 (Wilson), 27896 (Wilson), 27822 (Elm City), 27883 (Stantonsburg), 27880 (Sims), 27851 (Lucama), 27804 (Rocky Mount), 27803 (Rocky Mount), 27542 (Kenly), 27557 (Middlesex), 27597 (Zebulon)
Duration: 12-Month Contract
Mode of Interview: Mandatory Onsite Interview
Need Proper Linkedin and Local candidates only
Must Have:
- Bachelor's Degree in Life Sciences, Engineering, or related field
- 3+ years Validation experience in a Pharmaceutical/GMP environment
- Experience developing/reviewing/executing IQ/OQ/PQ protocols
- Equipment, Utilities, and Process Validation experience
- Strong knowledge of FDA, EMA, ICH, GAMP5
- Risk-Based Validation experience
- Validation Lifecycle Management experience
- Data Integrity knowledge
- Deviation Investigations & CAPA experience
- Validation Documentation experience
- Cross-functional collaboration with QA, QC, Engineering & Manufacturing
Strong Pluses:
- Veeva Vault
- SAP
- PAS-X
- Computer System Validation (CSV)
- CSA/Data Integrity requirements
- LEAN / Kaizen / Root Cause Analysis
- FMEA / HACCP Risk Assessments
Ideal Candidate Profile: Hands-on pharmaceutical validation professional with experience supporting equipment, utilities, process validation, IQ/OQ/PQ execution, deviation investigations, CAPAs, and maintaining validated GMP systems
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