Pharma Cleaning Validation Specialist (GMP)

United Pharma

Kentucky

On-site

USD 90,000 - 130,000

Full time

5 days ago
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Job summary

United Pharma in Kentucky is seeking an experienced Cleaning SME to support pharmaceutical cleaning validation efforts in a GMP-regulated manufacturing environment. The role focuses on developing and reviewing cleaning validation documentation, establishing robust strategies, and resolving validation-related challenges to ensure compliant operations.

You will collaborate with Manufacturing, QA, Validation, and Engineering teams to troubleshoot issues, review protocols, and implement effective

Qualifications

  • Pharma-cleaning validation experience required.
  • Strong GMP knowledge and documentation practices.
  • Ability to troubleshoot validation issues and implement corrective actions.
  • Experience developing and reviewing validation protocols and reports.

Responsibilities

  • Provide SME guidance on cleaning processes and validation activities in pharma manufacturing.
  • Support equipment and process cleaning per GMP and procedures.
  • Develop, review, and execute cleaning validation protocols and reports.
  • Identify worst-case products/equipment to set cleaning strategies.
  • Evaluate procedures to ensure suitability for equipment and processes.
  • Troubleshoot validation issues and recommend corrective actions.
  • Collaborate with Manufacturing, QA, Validation, and Engineering teams to resolve challenges.

Skills

Cleaning validation
GMP compliance
Documentation
Troubleshooting
Cross-functional collaboration

Job description

United Pharma in Kentucky is seeking an experienced Cleaning SME to support pharmaceutical cleaning validation efforts in a GMP-regulated manufacturing environment. The role focuses on developing and reviewing cleaning validation documentation, establishing robust strategies, and resolving validation-related challenges to ensure compliant operations.

You will collaborate with Manufacturing, QA, Validation, and Engineering teams to troubleshoot issues, review protocols, and implement effective

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