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Cleaning Validation Subject Matter Expert

Job in Chicago, Cook County, Illinois, 60290, USA
Listing for: Stark Pharma Solutions Inc
Full Time position
Listed on 2026-08-28
Job specializations:
  • Pharmaceutical
    Pharmaceutical Manufacturing, Quality Engineering
Salary/Wage Range or Industry Benchmark: 95000 - 135000 USD Yearly USD 95000.00 135000.00 YEAR
Job Description & How to Apply Below

Position:
Cleaning Validation Subject Matter Expert

Location:

Illinois

Duration:
Long Term

Job Overview

We are seeking an experienced Cleaning Validation Subject Matter Expert to lead cleaning validation activities in a GMP manufacturing environment. The role involves developing cleaning procedures, preparing and executing validation activities, troubleshooting cleaning-related issues, and providing technical expertise to support compliance with cGMP and FDA requirements.

Key Responsibilities
  • Design and develop cleaning procedures for manufacturing equipment and new products.
  • Provide technical support for manufacturing cleaning activities.
  • Lead cleaning validation activities and programs.
  • Support selection and use of cleaning agents and establish effective cleaning practices.
  • Develop and implement cleaning strategies for product transfer and product development projects.
  • Investigate cleaning-related deviations, incidents, and out-of-specification results.
  • Perform root-cause analysis and troubleshooting for cleaning issues.
  • Lead improvements to cleaning practices and review work instructions.
  • Support periodic review of cleaning validation studies.
  • Resolve incidents and deviations related to cleaning activities.
  • Initiate and manage change controls for cleaning procedure changes.
  • Collaborate with cross-functional teams to ensure timely completion of validation activities.
Required Qualifications
  • Bachelor s degree in Engineering, Science, or a related field.
  • 4+ years of experience in GMP manufacturing and cleaning validation.
  • Strong knowledge of cleaning validation principles and practices.
  • Experience with cleaning procedures, protocols, investigations, and change controls.
  • Familiarity with FDA regulatory requirements and cGMP standards.
  • Experience with continuous process improvement and equipment/process qualification.
  • Strong critical-thinking and technical-writing skills.
  • Strong communication, organizational, and cross-functional collaboration skills.
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