CQV Engineer - GMP Validation for Pharma Projects

Validation & Engineering Group, Inc.; San Francisco (CA); On-site; USD 90,000 - 130,000; Full time

Job summary

Validation & Engineering Group, Inc. in the San Francisco Bay Area is seeking a CQV Engineer to support a pharmaceutical/biotechnology project. Ideal candidates will have 2-4 years in commissioning, validation, or related engineering within regulated environments.

You will participate in FAT activities, review drawings, and ensure GMP compliance while coordinating with vendors and client teams on-site for the full project duration.

Qualifications

• Bachelor's degree in Engineering or related field.
• 2-4 years of CQV/validation/commissioning experience.
• Experience with FAT execution and documentation.
• Experience with vessels, piping, equipment, and drawings.
• On-site Bay Area work for the duration of the project.

Responsibilities

• Support FAT activities, including execution, documentation, and issue resolution.
• Provide project engineering support for vessels, piping, equipment, and related systems.
• Review and interpret engineering drawings, specifications, and technical documentation.
• Support equipment and system readiness activities per project requirements.
• Collaborate with engineering, CQV, vendors, and client teams to resolve technical issues.
• Ensure activities and documentation comply with GMP and project quality requirements.
• Participate in meetings, walkdowns, inspections, and other project activities.

Skills

CQV/validation

FAT execution

Engineering documentation

On-site work

Regulated industry knowledge

Education

Bachelor's degree in Engineering

Tools

Engineering drawings

Job description

Validation & Engineering Group, Inc. in the San Francisco Bay Area is seeking a CQV Engineer to support a pharmaceutical/biotechnology project. Ideal candidates will have 2-4 years in commissioning, validation, or related engineering within regulated environments.

You will participate in FAT activities, review drawings, and ensure GMP compliance while coordinating with vendors and client teams on-site for the full project duration.