Field CQV Validation Engineer for GMP Systems

United Pharma; California (MO); On-site; USD 75,000 - 120,000; Full time

Job summary

United Pharma is seeking a Validation Engineer (CQV) to support commissioning, qualification, and validation activities for GMP facilities, equipment, and critical systems in a regulated life sciences environment. This role emphasizes field presence and collaboration with cross-functional project teams to ensure systems are properly commissioned and ready for GMP operations.

The candidate will author and execute IQ, OQ, and PQ protocols, prepare validation documentation, and maintain cGMP

Qualifications

• 2–4 years of validation/CQV experience in regulated manufacturing environments.
• Hands-on equipment validation in life sciences facilities.
• Experience authoring and executing validation protocols.
• Knowledge of cGMP documentation and validation requirements.
• Ability to coordinate qualification activities with multiple teams.

Responsibilities

• Execute commissioning, qualification, and validation activities for GMP facilities and manufacturing systems.
• Develop, author, and execute IQ, OQ, and PQ protocols and validation documentation.
• Prepare validation protocols, summary reports, deviations, and protocol exceptions.
• Support qualification of facilities, cleanrooms, HVAC, and GMP utilities.
• Coordinate qualification schedules with Engineering, Manufacturing, and Quality.
• Review commissioning documentation and verify readiness prior to qualification testing.
• Maintain compliant validation documentation per cGMP requirements.
• Provide hands-on field support during startup, troubleshooting, and turnover.
• Participate in project meetings and provide CQV input.

Skills

CQV experience

GMP validation

Project coordination

Documentation

Job description

United Pharma is seeking a Validation Engineer (CQV) to support commissioning, qualification, and validation activities for GMP facilities, equipment, and critical systems in a regulated life sciences environment. This role emphasizes field presence and collaboration with cross-functional project teams to ensure systems are properly commissioned and ready for GMP operations.

The candidate will author and execute IQ, OQ, and PQ protocols, prepare validation documentation, and maintain cGMP