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

Dallas, TX, US • Posted 2 days ago • Updated 2 days ago
Contract W2
Contract Independent
Contract Corp To Corp
12 Months
No Travel Required
On-site
Depends on Experience
Fitment

Dice Job Match Score™

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Job Details

Skills

  • microbiological validations: Bioburden
  • Endotoxin
  • Sterility & PET.

Summary

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
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10211255
  • Position Id: 245748-14311-1788382085
  • Posted 2 days ago
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