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Validation Specialist - F2F

Tek Inspirations LLCStantonsburg, NC🇺🇸United StatesPosted 9 Sept 2026

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

Seniority
Mid Senior
Work mode
On Site
Location
Stantonsburg, NC, United States
Posted
22 hours ago
HACCPKaizenRoot Cause AnalysisSAPVault

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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