Article | MED DEVICE ON LINE 

 

ABOUT THE AUTHOR

Leo Gelera, Quality Manager

Leo joined FMI in March of 2012. Leo began his career in medical device manufacturing specifically working for Abbott and Baxter Healthcare. He dedicated his time to various quality roles focusing on Quality System Improvements, Regulatory Compliance, and Lean Six Sigma Disciplines. He is a Certified Lead Auditor to the International Organization for Standards specific to medical devices as well as the FDA Code of Federal Regulation Requirements. Leo brings 15 years of quality experience to FMI. He holds an Executive MBA in Risk Management from Colorado State University and is the appointed Quality Management Representative for the FMI establishment.

 

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