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Technical Lead II – GxP Validation- Onsite at Dallas, TX and need Local to Texas

E-Solutions, Inc.Dallas, TX🇺🇸United StatesPosted 7 Sept 2026

Why This Role Stands Out

This role offers significant growth in GxP validation, allowing you to deepen your expertise in a reputable company. You'll thrive here if you are a detail-oriented professional eager to contribute to critical pharmaceutical processes and collaborate with cross-functional teams. Apply today to advance your career in this impactful position!

Quick Overview

Seniority
Mid Senior
Work mode
On Site
Location
Dallas, TX, United States
Posted
2 days ago
Scheduling

Job Description

Hi Professionals,

Title: Technical Lead II – GxP Validation

Location: Fort Worth, Texas — 100% onsite, 5 days/week

JD:
 

Main Responsibilities

  • Perform microbiological validations: Bioburden, Endotoxin, Sterility & PET.
  • Support QC Microbiology laboratory operations.
  • Conduct equipment qualifications and support Media Fill/Reads.
  • Identify quality issues, troubleshoot, and implement corrective actions/improvements.
  • Prepare protocols, reports, and SOPs as required.
  • Follow GxP/GDP and pharmaceutical regulatory requirements.
  • Collaborate with Production, Maintenance, Warehouse, and other departments.
  • Support training, scheduling, supplies, and overall lab workflow.

 

 

Key Qualifications

  • Bachelor’s degree or equivalent relevant experience.
  • Strong knowledge of pharmaceutical/GxP regulatory requirements.
  • Excellent written and verbal communication.
  • Detail-oriented, proactive, and able to manage multiple projects independently.
  • Comfortable working overtime/flexible hours when required.

Technical Lead II – GxP Validation- Onsite at Dallas, TX and need Local to Texas1validation,QC Microbiology,microbiological validations,Bioburden,Endotoxin,Sterility,PET,GxP/GDPN/AC2CUnited States

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