Carol Brennon Tousey

Owner and Primary Consultant, Compliance, Quality, Technical

Carol Brennon Tousey is a skilled professional, working in Carol Tousey Consulting as a Owner and Primary Consultant, Compliance, Quality, Technical since 2020. Carol gained professional experience in more than five positions at various companies. Carol Brennon Tousey went to the University of New Hampshire and was studying from 2000 to 2003. Charleston, South Carolina is the city, where the professional was lastly known to settle. This professional's email address and phone number are easily accessed through this website on demand.
Name variants:
Carrol Tousey, Carroll Tousey, Carole Tousey, Karol Tousey, Carrie Tousey, Carry Tousey

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Contact Information

Last Update
Jul 1, 2022
Email
ca**@nutramfg.com
Location
Charleston, SC
Company
Carol Tousey Consulting

Workplace

Owner and Primary Consultant, Compliance, Quality, Technical

Work History

Owner and Primary Consultant, Compliance, Quality, Technical

from Apr 2020

Senior Lead Auditor and Regulatory Affairs Manager

Second and third party audits, dispute & appeals panel, certification decisions, technical report review
Feb 2009 — Jan 2014

Senior Lead Auditor, External Quality

1050 Woodruff Rd, Greenville, SC 29607
from Jan 2014

Qa and Regulatory Affairs, Quality Systems Consultant

Created and administered training programs for regulatory compliance, quality systems consulting, regulatory affairs liason
May 2007 — Jul 2011

Qa and Qc and Regulatory Affairs

89 Bridge St, Lancaster, NH 03584
Creating and managing self-directed work teams, material review board, executive management and strategic planning, created training programs, internal and external audit programs, supplier ...
Apr 1994 — May 2007

Education

1987 — 1989

Occupations

Executive
Owner
Counselor
Accountant
Auditor
Manager
Chief Executive
Advisor
Operations Manager

Skills

Quality Assurance
Regulatory Affairs
Project Management
Strategic Planning
Collaborative Problem Solving
Quality Auditing
Vendor Management
Training
Gmp
Management
Validation
Fda
Regulatory Requirements
Medical Devices
Change Control
Auditing
Quality Management
Quality System
V&V
Sop
Standard Operating Procedure
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