×
Register Here to Apply for Jobs or Post Jobs. X

Validation Engineer

Job in Fort Worth, Tarrant County, Texas, 76102, USA
Listing for: Stark Pharma
Full Time position
Listed on 2026-06-19
Job specializations:
  • Pharmaceutical
    Validation Engineer, Pharma Engineer, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Job Title:

Validation Engineer

Location:

Fort Worth, TX (Local candidates only)

Travel:
Required Alabama (3 4 weeks, expenses paid)

Duration: 3 6 Month Contract

Start Date:

Immediate

Job Summary

We are seeking a Validation Engineer to support EO sterilization validation activities within a regulated manufacturing environment. This role will focus on supervising and coordinating Performance Qualification (PQ) execution activities while ensuring compliance with GMP and ALCOA+ documentation standards.

The ideal candidate will have hands‑on experience with sterilization validation processes, strong coordination skills, and the ability to support cross‑functional execution activities in a fast‑paced environment.

Key Responsibilities
  • Supervise execution of EO sterilization Performance Qualification (PQ) activities
  • Coordinate half-cycle, nominal/full-cycle, and maximum-cycle sterilization runs
  • Prepare and manage PCDs (Process Challenge Devices) and Biological Indicators (BIs) for shipment and cycle insertion
  • Support preparation and arrangement of dunnage for EO sterilization processes
  • Oversee movement of product loads through refrigerated storage, tempering, sterilization, and aeration processes
  • Coordinate retrieval and shipment of PCDs, BIs, and product samples for Quality Control testing
  • Ensure execution activities and documentation comply with ALCOA+ principles and GMP requirements
  • Collaborate with Validation, Quality, and Operations teams to support project timelines and execution
Required Qualifications
  • Experience in validation within medical device, pharmaceutical, or regulated manufacturing environments
  • Hands‑on knowledge of EO sterilization validation and PQ execution activities
  • Strong understanding of GMP documentation practices and ALCOA+ principles
  • Ability to coordinate cross‑functional activities and manage execution timelines
  • Strong communication and organizational skills
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary