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Utility Validation Engineer

Job in Chicago, Cook County, Illinois, 60290, USA
Listing for: Stark Pharma Solutions Inc
Full Time position
Listed on 2026-08-24
Job specializations:
  • Engineering
    Validation Engineer, Quality Engineering, Pharma Engineer
Salary/Wage Range or Industry Benchmark: 85000 - 120000 USD Yearly USD 85000.00 120000.00 YEAR
Job Description & How to Apply Below

Job Overview

We are seeking a Utility Validation Engineer to support utility system validation and qualification activities in a GMP manufacturing environment. The role involves leading qualification activities, preparing validation documentation, supporting commissioning, and collaborating with Engineering, Quality, Manufacturing, and other cross-functional teams to ensure compliance with cGMP and FDA requirements.

Position

Utility Validation Engineer

Location

Illinois

Duration

Long Term

Key Responsibilities
  • Author specifications and supporting documentation, including URS, RA, and FS.
  • Lead commissioning testing for GMP utility systems.
  • Develop and execute IQ/OQ/PQ qualification protocols.
  • Support qualification of WFI and Purified Water systems.
  • Lead qualification of clean steam, compressed air, and process gas systems.
  • Perform temperature mapping and airflow/smoke studies for HVAC and cleanroom qualification.
  • Use Kaye Validators and temperature/humidity data loggers for qualification activities.
  • Manage multiple qualification activities, schedules, and deliverables.
  • Lead cross-functional meetings and document meeting notes and action items.
  • Support project forecasting and planning for upcoming qualification activities.
  • Collaborate with Engineering, Process, and Production teams to resolve technical issues.
  • Provide technical expertise and recommend process improvements.
  • Maintain compliance with cGMP, FDA requirements, company policies, and safety procedures.
Required Qualifications
  • Bachelor s degree in Engineering, Science, or a related field.
  • 2 5 years of experience in GMP utility validation or qualification.
  • Experience with WFI, Purified Water, clean steam, compressed air, and HVAC systems.
  • Experience with Kaye Validators and temperature/humidity data loggers.
  • Experience working in a GMP manufacturing environment.
  • Experience preparing SOPs, validation protocols, and technical reports.
  • Knowledge of FDA regulatory requirements and cGMP standards.
  • Strong critical-thinking and technical-writing skills.
  • Strong communication, organizational, and cross-functional collaboration skills.
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