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