Cleaning Validation Engineer | Biotech/Pharma CIP Expert

Hyde Engineering + Consulting; City of Syracuse (NY); On-site; USD 85,000 - 120,000; Full time

Job summary

Hyde Engineering + Consulting in the United States seeks a Cleaning Validation Engineer to lead cleaning and process validation in biopharma settings, generating, executing and reporting tests across commissioning and qualification phases.

The role requires CIP/COP and manual cleaning validation, troubleshooting CIP systems, developing CIP/COP cycles, and preparing SOPs and reports while ensuring adherence to project scope, timelines and GMP policies.

Qualifications

• Experience with CIP/COP and manual cleaning validation activities is required.
• Ability to analyze data, determine results and present conclusions.
• Experience developing documents and SOPs.
• Strong written and verbal communication for cGMP environments.
• Experience in discrepancy and non-conformance reporting and root cause analysis is preferred.

Responsibilities

• Generate, execute and report testing for commissioning and qualification phases.
• Post-cleaning validation monitoring and cleaning cycle development in a cGMP facility.
• Review GxP deliverables including specifications, drawings, and validation documentation.
• Train operations staff on protocols and technical details.
• Organize, schedule and track validation projects to meet timelines.

Skills

Problem solving

Technical reading

Cross-functional teamwork

Verbal and written communication

Project management

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Microsoft Visio

Tools

CIP systems

SIP systems

cabinet washers

COP

manual cleaning

Job description

Hyde Engineering + Consulting in the United States seeks a Cleaning Validation Engineer to lead cleaning and process validation in biopharma settings, generating, executing and reporting tests across commissioning and qualification phases.

The role requires CIP/COP and manual cleaning validation, troubleshooting CIP systems, developing CIP/COP cycles, and preparing SOPs and reports while ensuring adherence to project scope, timelines and GMP policies.