Validation Engineer - Los Angeles, United States - Redbock - an NES Fircroft company

Description

A specialized Medical Device CDMO in Northern LA, CA is in immediate need of a

Validation Engineer for a 6-month project . The project needs to be completed while working

every day onsite .

The client company is growing rapidly and there is now a growing list of pieces of

lab equipment

that need to be qualified in support of a backlog. The Validation Engineer needs to be an expert with lab equipment like Agilent


HPLCs, GCs, centrifuges, and Analytical Balances

among other types of instruments.

Top Requirements

:

5+ years of direct lab experience validating lab equipment, this experience must be clearly detailed in CV
5+ years of experience as a Validation Engineer working with Medical Device and Pharmaceutical companies
BS degree minimum
Strong knowledge of FDA standards and regulations, especially regulations for labs
Strong experience working in a lab setting to qualify a range of equipment/instruments like:


HPLC
GC / GC Headspace Sampler
Microbalances / Analytical balances
Centrifuges
Strong expertise reading User Requirements from vendors and translating them to protocols for qualification
Experience communicating with equipment vendors
Must be an expert in developing and executing validation protocols (IQ/OQ/PQs)
Strong communication skills and a team player

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