Jobs · Quality Assurance · Illinois

Utility Validation Engineer

Stark Pharma Solutions Inc · Chicago, IL · 1 wk ago
On-siteQuality AssuranceFull-time

About the Role

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.

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.

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.

Location: Illinois
Duration: Long Term

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