CQV Engineer II: GMP Validation Life Sciences
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Engineering
Job Description & How to Apply Below
IPS-Integrated Project Services in Emeryville, CA is seeking a CQV Engineer II to perform commissioning, qualification, and validation activities for life sciences facilities.
You will write and witness CQV documents, conduct field activities, and support CSV/automation projects, with up to 100% travel as required. A BS in Engineering and 2+ years of relevant experience in pharma/biotech/medical devices are expected.
The following role is for a CQV Engineer II: GMP Validation for Life Sciences with IPS-Integrated Project Services, LLC.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Emeryville, CA, United States.
This opportunity is part of our work in Engineering.
The advertised compensation is 96..
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