Betsy Cortelloni

Director

Since 2019, Betsy Cortelloni has been working in Femasys situated 17, 17. This person is a well-qualified Director with over 27 years of work experience. According to Betsy's resume and work profile, this expert has worked at more than nine places with numerous backgrounds and got various skills. Betsy attended school at the Keller Graduate School of Management of Devry University from 1994 to 1996. Betsy has professional certification in Regulatory Affairs Certified and Regulatory Affairs Professional Society. Betsy can be found in Atlanta, Georgia – where the professional is currently located. You can search for this person's email address and phone. We can also provide you with additional contact information upon request.
Name variants:
Elizabeth Cortelloni
Last updated Jun 17, 2024

Contact Information

Last Update
Jul 9, 2022
Email
bc**@bellsouth.net, co**@theragenics.com, co**@theragenics.com
Location
Atlanta, GA
Company

Workplace

Femasys
Director

Suwanee, GA

Industry

Medical Devices, Mfg Surgical Appliances/Supplies

Work History

Director

3950 Johns Creek Ct SUITE 100, Suwanee, GA 30024
from Jul 2019

Corporate Director of Quality and Regulatory Affairs

5203 Bristol Industrial Way, Buford, GA 30518
Oversee the quality systems and regulatory affairs for a corporate family of 4 medical device companies.
Mar 2011 — Jul 2019

Director of Quality and Regulatory Affairs

5203 Bristol Industrial Way, Buford, GA 30518
Mar 2008 — Mar 2011

Regulatory Affairs Manager

5203 Bristol Industrial Way, Buford, GA 30518
Feb 2004 — Mar 2008

Manager of Regulatory Affairs and Product Assurance

May 1997 — Jun 2003

Regulatory Affairs Manager

Nov 1995 — Jan 1997

Supervior of Quality Complaints and Returns

Jan 1993 — Nov 1995

Regulatory Affairs Specialist

1991 — 1993

Ra Manager

5203 Bristol Industrial Way, Buford, GA 30518

Occupations

Executive
Manager
Operations Manager

Skills

Quality System
Medical Devices
Regulatory Affairs
Fda
Iso 13485
Design Control
Quality Assurance
Capa
Validation
Gmp
Iso
Ce Marking
Quality Auditing
Process Improvement
Iso 14971
R&D
Sop
Manufacturing
Product Development
Change Control
21 Cfr
Fda Gmp
Regulatory Submissions
Medical Device Directive
Risk Management
Fmea
Biomedical Engineering
21 Cfr Part 11
Mergers and Acquisitions
Process Validation
Quality Systems
Qsr
510 K
Compliance
Mergers
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