Pharma CQV Engineer: Validation & CIP Systems

United Pharma; Ohio; On-site; USD 85,000 - 120,000; Full time

Job summary

United Pharma seeks a CQV Consultant to support commissioning, qualification, and validation across pharmaceutical manufacturing systems, including CIP systems and manufacturing support equipment.

You will perform system walkdowns, develop IQ/OQ/PQ protocols, prepare qualification reports, and provide process engineering support while ensuring cGMP compliance. This role requires collaboration with project teams to deliver timely, compliant results.

Qualifications

• Bachelor's degree in Chemical Engineering or related field (or equivalent experience).
• Minimum 1 year in commissioning, qualification and validation within pharma/manufactured environment.
• Experience with system walkdowns, P&ID reviews, and qualification execution.
• Knowledge of IQ, OQ, PQ protocols, documentation and final reporting.
• Familiarity with CIP systems and pharmaceutical process equipment.
• Strong written and verbal communication skills; able to multitask in fast-paced projects.
• Ability to collaborate across project teams, quality and engineering.

Responsibilities

• Perform system walkdowns, P&ID reviews, equipment commissioning, and ETOP prep.
• Execute C&Q activities for pharmaceutical process systems and equipment.
• Develop IQ, OQ, PQ protocols and prepare final qualification reports.
• Provide process engineering support for CIP systems and equipment.
• Review system documentation, data packages, calibration certificates, and trends.
• Support project lead in coordinating deliverables and schedules.
• Track and report project progress to meet timelines and scope.
• Maintain qualification documentation, protocols, reports and records.
• Identify issues and support timely troubleshooting and resolution.
• Promote cGMP practices and regulatory compliance.

Skills

Communication

Collaboration

Project coordination

Education

Bachelor's degree in Chemical Engineering

Tools

IQ/OQ/PQ protocols

Job description

United Pharma seeks a CQV Consultant to support commissioning, qualification, and validation across pharmaceutical manufacturing systems, including CIP systems and manufacturing support equipment.

You will perform system walkdowns, develop IQ/OQ/PQ protocols, prepare qualification reports, and provide process engineering support while ensuring cGMP compliance. This role requires collaboration with project teams to deliver timely, compliant results.