Tom Brooks personal email
- Valid
Manufacturing and Validation Engineer with over 28 years of experience in the medical device manufacturing and pharmaceutical industry. Managed all software and hardware validation activities of manufacturing equipment, laboratory equipment, and Information Technology per 21CFR Part 11 and 211, and GAMP. Involved in the R&D, manufacturing, and support for all levels of a medical device’s life cycle complying with standards set by specific regulatory bodies around the world, such as the U.S. Food and Drug Administration (FDA) in conjunction with Good Manufacturing Practices (GMP) and Quality Systems (QS) Regulations.
Validation Engineering Services (Ves)
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Owner And Principal Validation EngineerValidation Engineering Services (Ves)Bend, Or, Us
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Owner & Principal Validation EngineerValidation Engineering Services (Ves) Dec 2018 - Present
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Validation Operations ManagerCsa Soliance Dec 2010 - Dec 2018CSA Soliance offers practical, science-based solutions for process and software validation, process automation and laboratory support to FDA-regulated life science companies. We specialize in risk management techniques that ensure operational reliability and compliance while managing the cost of quality
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Validation EngineerHospira Mar 2007 - Dec 2010Lake Forest, Il, Us -
Manufacturing EngineerAlcon Nov 1990 - Dec 2006Geneva, Switzerland, Ch
Tom Brooks Skills
Tom Brooks Education Details
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California State University, Long BeachIndustrial Technology - Electronics
Frequently Asked Questions about Tom Brooks
What company does Tom Brooks work for?
Tom Brooks works for Validation Engineering Services (Ves)
What is Tom Brooks's role at the current company?
Tom Brooks's current role is Owner and Principal Validation Engineer.
What is Tom Brooks's email address?
Tom Brooks's email address is t8****@****ail.com
What schools did Tom Brooks attend?
Tom Brooks attended California State University, Long Beach.
What skills is Tom Brooks known for?
Tom Brooks has skills like Reliability Engineering, Cleaning Validation, Validation, Capital Equipment, Capa, Iso 13485, Change Control, Design Control, Quality Auditing, Quality System, Fda, V&v.
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