Keith Morel is a highly qualified professional, working in Usc School of Pharmacy as a Adjunct Assistant Professor, Department of Regulatory and Quality Sciences from 2019. Keith gained professional experience in more than ten positions at various companies. Keith Morel went to the Dyson School of Design Engineering and received education there from 1995 to 1999. This person has such qualifications as Asq Certified Biomedical Auditor, License 1047, and Asq, License 1047. Belmont, California is the city, where this professional was lastly known to be living. The person's email address and phone are accessed through this website by request.
Name variants:
Keith Morel
Last updated May 31, 2024
Contact Information
Last Update
Jul 13, 2022
Email
ke**@qservegroup.com, ke**@hotmail.com
Location
Belmont, CA
Company
Usc School of Pharmacy
Workplace
Adjunct Assistant Professor, Department of Regulatory and Quality Sciences
Work History
Adjunct Assistant Professor, Department of Regulatory and Quality Sciences
Teaching and course development in the RegSci program at USC.
from Jul 2019
Usc Regulatory Science, Course Instructor
Instructor for the 2 unit (32 classroom-hour) course "Quality Systems and Statistical Process Control" (RSCI 507), which is part of the MS in Medical Product Quality.
from Oct 2016
Vice President of Regulatory Compliance at Qserve Group Us Inc
Assist medical device manufacturers with the CE marking process in order to gain access to the European market, as well as addressing their general strategic and tactical RA/QA/CA questions ...
from Nov 2015
Senior Director of Regulatory Compliance
1310 Chesapeake Ter, Sunnyvale, CA 94089
Mar 2014 — Oct 2015
Usc Regulatory Science, Guest Lecturer
Guest lecture in the MPTX Global Regulation of Medical Products course (which is part of the MS in Regulatory Science program).
Lectures:
Working with a Notified Body
Standards .... and ...
from Nov 2010
Director, Research and Development
Managed R&D activities throughout the Oculus organization (USA, Mexico & The Netherlands) Developed R&D strategy to meet all business, regulatory, quality and marketing requirements Develope...
Mar 2004 — Mar 2005
Manager, Ivus Disposable Development; Senior Scientist, Ivus Transducer Development
Jun 2000 — Mar 2004
Doctoral Research Associate
Worked with emissive and Langmuir probes to diagnose an arc plasma. Daily working language was French.
Nov 1999 — Mar 2000
Education
1995 — 1999
1992 — 1995
Occupations
Executive
Vice President
Professor
Associate Professor
Adjunct Instructor
Instructor
Pedagogue
Master of Science
Chief Executive
Lecturer
Postsecondary Teacher
Skills
Iso 13485
Medical Devices
Design Control
Quality System
Validation
R&D
Regulatory Affairs
Iso 14971
V&V
Capa
Quality Management
Quality Assurance
Iso
Quality Auditing
Quality Control
Gmp
Biomedical Engineering
Ce Marking
Medical Device Directive
Verification and Validation
Manufacturing
Risk Management
Product Development
Fmea
Quality Systems
Iso Standards
Corrective and Preventive Action
Testing
21 Cfr Part 11
Research and Development
Clinical Evaluation For Medical Devices
Design of Experiments
Regulatory Submissions
Design Dossiers
Combination Devices
Statistical Data Analysis
Process Simulation
Cardiovascular Devices
Dmaic