Job Description
Technical Source is hiring a hands-on Validation Engineer to support commissioning and qualification activities at a rapidly growing biotech manufacturing site in Durham. This is not a paper-pusher role, we’re looking for someone who can be in the field, write solid protocols, execute IQ/OQ, and drive equipment to operational readiness.
If you’ve validated lab equipment, supported cleaning validation, and know your way around cGMP documentation, keep reading.
What You’ll Be Doing
Writing and executing IQ/OQ protocols
Supporting equipment startup, FAT/SAT, and commissioning
Redlining and developing URS / FRS / DDS documentation
Driving lifecycle documentation through approval
Supporting change control, deviations, and CAPAs
Working side-by-side with Engineering, QA, Manufacturing, and Vendors
Ensuring compliance with 21 CFR 210, 211, a...
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