Utility Validation Engineer
Job in
Chicago, Cook County, Illinois, 60290, USA
Listed on 2026-08-24
Listing for:
Stark Pharma Solutions Inc
Full Time
position Listed on 2026-08-24
Job specializations:
-
Engineering
Validation Engineer, Quality Engineering, Pharma Engineer
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.
PositionUtility Validation Engineer
LocationIllinois
DurationLong 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.
- 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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