CQV Engineer
Validation and Engineering Group, Inc
Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
Responsibilities
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
- CQV Engineer
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.
- 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.
- Commissioning & Qualification (C&Q/CQV)
- Factory Acceptance Testing (FAT)
- Equipment and utility systems
- Piping and mechanical systems
- Engineering drawings and specifications
- GMP-regulated environments
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.
Vacancy posted 2 days ago
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