Mike Morrell

Greater Minneapolis-St Paul Area

Mike Morrell is a high-level expert, working in Uroplasty, Inc as a Director of Regulatory Affairs and Quality Assurance. This expert gained professional experience in more than two positions at different companies. Mike Morrell went to the St. John's University and got education from 1986 to 1990. Minneapolis, Minnesota is the area, where this professional was lastly known to settle. This professional's phone number and email can be easily accessed through Connexy by request.
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Michael Morrell

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Contact Information

Last Update
Jul 10, 2022
Email
mi**@uroplasty.com
Location
Minneapolis, MN
Company
Uroplasty, Inc.

Workplace

Director of Regulatory Affairs and Quality Assurance

Work History

Director of Regulatory Affairs and Quality Assurance

Director of Regulatory Affairs

Greater Minneapolis-St. Paul Area
Feb 2000 — Aug 2006

Education

1986 — 1990

Occupations

IT Professional
Software Tester
Executive
Director
Computer Specialist
Operations Manager

Skills

Clinical Trials
Quality Assurance
Design Control
Clinical Research
Capa
Gcp
Quality System
Regulatory Affairs
Medical Devices
Fda
Product Development
Iso 13485
Biotechnology
Urology

FAQs about Mike Morrell

What is the main profession of Mike Morrell?

Mike is a Greater Minneapolis-St Paul Area.

What jobs is Mike a professional at?

The expert is a professional IT Professional and Software Tester jobs.

Where does Mike Morrell currently live?

Minneapolis, Minnesota is the place where Mike Morrell lives

What is Mike Morrell's email?

The expert's email is mi**@uroplasty.com.

Where did Mike Morrell work?

This person worked at Uroplasty, Inc., Uroplasty, Inc..

What education does Mike Morrell have?

Mike studied at the St. John's University from 1986 to 1990.

Are there any special industries, that Mike Morrell is connected to?

Mike Morrell works in Medical Devices industry.

Are there any special skills Mike Morrell has?

This professional has the following skills: Clinical Trials, Quality Assurance, Design Control, Clinical Research, Capa, Gcp, Quality System, Regulatory Affairs, Medical Devices, Fda, and Product Development.
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