Quality, Processor Validation Eng. CAPA specialist

Hello and thank you for reviewing my Resume

I have over 20 years experience developing and implements optimal, cost-effective manufacturing processes and methods in accordance with product specifications and quality standards. Most of this experience has been in Medical Device manufacturing. That experience includes processing and packaging of a variety of medical device and pharmaceutical products.
My Process, Compliance and Quality experience focus has been over the last 8 years. Most recently I worked as a contact Compliance Quality Technology Engineer for Maetrics.
My Process Engineering tool box includes: IQ, OQ, PQ, Teaching and auditing to cGMPs/QSRs, Process Improvement, Problem Resolution, Project Management & Employee Training as an integral part of my career experiences along with improving manufacturing processes and methods for cost-reduction, quality improvement and efficiency.
Thank you for your consideration.
Sandy, Utah

This example was posted: 3/23/2011 10:39:42 PM EST

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