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Validation & Engineering Group is seeking a CQV Engineer to support a pharmaceutical/biotechnology project in the Bay Area. The ideal candidate will have 24 years of experience in commissioning, qualification, validation, or project engineering within a regulated industry.
The role involves FAT execution, documentation, and collaboration with vendors and client teams to ensure GMP compliance and project quality. On-site work in the Bay Area is expected for the duration of the project.
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 CQV Engineer
We are seeking a CQV Engineer to support a pharmaceuticalbiotechnology project in the Bay Area The ideal candidate will have 24 years of experience in commissioning qualification validation or project engineering within a regulated industry
Support FAT Factory Acceptance Testing activities including execution documentation and issue resolutionProvide project engineering support for vessels piping equipment and related systemsReview and interpret engineering drawings specifications and technical documentationSupport equipment and system readiness activities in accordance with project requirementsCollaborate with engineering CQV vendors and client teams to identify and resolve technical issuesEnsure activities and documentation comply with applicable GMP and project quality requirementsParticipate in meetings walkdowns inspections and other project activities as required
Bachelors degree in Engineering or a related technical discipline preferred24 years of experience in CQV validation commissioning project engineering or a related fieldExperience with FAT execution and technical documentationKnowledge of vessels piping equipment and engineering drawingsPharmaceutical biotechnology medical device or other regulated industry experience preferredStrong technical documentation communication and problem solving skillsAbility to work on site in the Bay Area 40 hours per week for the duration of the project
Commissioning & Qualification C&QCQVFactory Acceptance Testing FATEquipment and utility systemsPiping and mechanical systemsEngineering drawings and specificationsGMP regulated environments
At Validation & Engineering Group people always come first We believe that when youre empowered to do your best work bold ideas thrive and real progress happens This isnt just a job its 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
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