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2016-01-28T00:00:00.000Z

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Wrong Max Mortensen?

Mr. Max Mortensen K.

Vice President of Global Quality, Clinical and Regulatory Affairs

Wright Medical Technology , Inc.

Direct Phone: (901) ***-****       

Email: m***@***.com

Wright Medical Technology , Inc.

5677 Airline Road

Arlington, Tennessee 38002

United States

Company Description

Wright Medical Technology, Inc., headquartered in Arlington, Tenn., is a global orthopedic medical device company specializing in the design, manufacturing and marketing of reconstructive joint devices and biologics. Wright's products include large joint ... more

Find other employees at this company (1,668)

Background Information

Employment History

Vice President Global Operations and Product Support

MicroPort Orthopedics Inc

Senior Director of Engineering, Operations, Safety, Etc

Bend Research Inc

Education

Ph.D. degree
Chemical Engineering
University of Southern California

Web References (28 Total References)


Max ...

www.sec.gov [cached]

Max Mortensen

...
Max Mortensen became our Vice President, Global Quality, Regulatory & Clinical in May 2011. Mr. Mortensen previously served as Vice President, Global Quality Systems since February 2010. He joined us in 2008 to lead our Advanced Engineering and Manufacturing program. Prior to joining us, Mr. Mortensen served as Director of Engineering for Bend Research Inc. from 2004 to 2008.


Max ...

www.sec.gov [cached]

Max Mortensen

...
Max Mortensen became our Vice President, Global Quality, Regulatory & Clinical in May 2011. Mr. Mortensen previously served as Vice President, Global Quality Systems since February 2010. He joined us in 2008 to lead our Advanced Engineering and Manufacturing program. Prior to joining us, Mr. Mortensen served as Director of Engineering for Bend Research Inc. from 2004 to 2008.


Wright Medical Technology | Investor Relations | Management Team & Directors

phx.corporate-ir.net [cached]

Max K. Mortensen - Vice President, Quality, Clinical & Regulatory Affairs

...
Max K. Mortensen Vice President, Quality, Clinical & Regulatory Affairs
Max K. Mortensen began serving as Wright's Vice President, Quality, Clinical & Regulatory Affairs in May 2011. He had previously served as Vice President, Global Quality Systems since February 2010. He joined the Wright team in 2008 to lead the Company's Advanced Engineering and Manufacturing program. His career prior to Wright includes 12 years in the pharmaceutical industry and extensive experience in R&D, manufacturing, operations, engineering, safety, design, scale-up and process engineer... 


Max K. Mortensen - Vice President, ...

phx.corporate-ir.net [cached]

Max K. Mortensen - Vice President, Quality, Clinical & Regulatory Affairs Wright Medical Technology | Investor Relations | Biography

...
Max K. Mortensen Vice President, Quality, Clinical & Regulatory Affairs
Max K. Mortensen began serving as Wright's Vice President, Quality, Clinical & Regulatory Affairs in May 2011. He had previously served as Vice President, Global Quality Systems since February 2010. He joined the Wright team in 2008 to lead the Company's Advanced Engineering and Manufacturing program. His career prior to Wright includes 12 years in the pharmaceutical industry and extensive experience in R&D, manufacturing, operations, engineering, safety, design, scale-up and process engineering functions. Mr. Mortensen holds a Ph.D. degree in Chemical Engineering from the University of Southern California.


Wright Medical Technology | Investor Relations | Management Team & Directors

phx.corporate-ir.net [cached]

Max K. Mortensen - Vice President, Quality, Clinical & Regulatory Affairs

...
Max K. Mortensen Vice President, Quality, Clinical & Regulatory Affairs
Max K. Mortensen began serving as Wright's Vice President, Quality, Clinical & Regulatory Affairs in May 2011. He had previously served as Vice President, Global Quality Systems since February 2010. He joined the Wright team in 2008 to lead the Company's Advanced Engineering and Manufacturing program. His career prior to Wright includes 12 years in the pharmaceutical industry and extensive experience in R&D, manufacturing, operations, engineering, safety, design, scale-up and process engineer... 

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