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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.
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:
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.
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.
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.