We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
We are seeking a
CQV Engineer to support a pharmaceutical/biotechnology project in the Bay Area. The ideal candidate will have
2• 4 years of experience in commissioning, qualification, validation, or project engineering within a regulated industry.
Responsibilities
- Support FAT (Factory Acceptance Testing) 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 in accordance with project requirements.
- Collaborate with engineering, CQV, vendors, and client teams to identify and resolve technical issues.
- Ensure activities and documentation comply with applicable GMP and project quality requirements.
- Participate in meetings, walkdowns, inspections, and other project activities as required.
Qualifications
- Bachelor's degree in Engineering or a related technical discipline preferred.
- 2• 4 years of experience in CQV, validation, commissioning, project engineering, or a related field.
- Experience with FAT execution and technical documentation.
- Knowledge of vessels, piping, equipment, and engineering drawings.
- Pharmaceutical, biotechnology, medical device, or other regulated-industry experience preferred.
- Strong technical documentation, communication, and problem-solving skills.
- Ability to work on-site in the Bay Area, 40 hours per week, for the duration of the project.
Preferred Experience
- Commissioning & Qualification (C&Q/CQV)
- Factory Acceptance Testing (FAT)
- Equipment and utility systems
- Piping and mechanical systems
- Engineering drawings and specifications
- GMP-regulated environments
