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.
Numbers & Facts
Location
Chicago, IL
Skills
Change Controlunmatched
Change Managementunmatched
Communication Skillsunmatched
Cross-Functionalunmatched
Current Good Manufacturing Practice (cGMP)unmatched
FDA Requirementsunmatched
GMP (Good Manufacturing Practices)unmatched
Identify Issuesunmatched
Manufacturingunmatched
Manufacturing Equipmentunmatched
Organizational Skillsunmatched
Procedure Developmentunmatched
Process Improvementunmatched
Product Developmentunmatched
Root Cause Analysisunmatched
Team Playerunmatched
Technical Supportunmatched
Technical Writingunmatched
Time Managementunmatched
Writing Skillsunmatched
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