Senior Validation Engineer: CQV Lifecycle in Pharma

Energy Jobline ZR; Milford (OH); On-site; USD 110,000 - 170,000; Full time

Job summary

Energy Jobline ZR is seeking a Principal Validation Engineer to lead lifecycle qualification of manufacturing facilities and develop CQV protocols across DQ, FAT, SAT, and IOPQ. The role requires strong hands-on validation in pharma/biotech, with three or more years managing cross-functional projects.

The candidate will oversee ed validation of cleaning processes and ensure all systems remain in a validated state, driving quality and compliance throughout the lifecycle.

Qualifications

• Bachelor’s degree in engineering or related field.
• 7+ years validation experience in pharma/biotech.
• 3+ years project management experience.
• Experience with cleaning validation and CQV lifecycle.

Responsibilities

• Perform lifecycle qualification of manufacturing facilities.
• Develop and execute CQV protocols and reports.
• Demonstrate hands-on validation of equipment and processes.
• Lead cross-functional validation projects.

Skills

Project management

Technical writing

Cross-functional collaboration

Quality systems

Education

Bachelor's degree in engineering or related field

Job description

Energy Jobline ZR is seeking a Principal Validation Engineer to lead lifecycle qualification of manufacturing facilities and develop CQV protocols across DQ, FAT, SAT, and IOPQ. The role requires strong hands-on validation in pharma/biotech, with three or more years managing cross-functional projects.

The candidate will oversee ed validation of cleaning processes and ensure all systems remain in a validated state, driving quality and compliance throughout the lifecycle.