Cynthia Merrell is a high-level professional, working in Vital Connect, Inc main office of which is in 1300. as a Vice President Quality and Regulatory from 2018. This person has earned professional experience in more than ten positions at different companies. Cynthia Merrell went to the University of California, Berkeley and received education there from 1984 to 1987. San Francisco, California is the area, where the professional was known to be settled. This person's contacts are easily accessed through this website by request.
Name variants:
Cindy Merrell,
Cyndi Merrell
Last updated Apr 30, 2024
Contact Information
Last Update
Jul 1, 2022
Email
cm**@vitalconnect.com, cm**@eneura.com, cy**@yahoo.com
Location
San Francisco, CA
Company
Vital Connect, Inc.
Workplace
Vice President Quality and Regulatory
Work History
Vice President Quality and Regulatory
224 Airport Pkwy SUITE 300, San Jose, CA 95110
from Oct 2018
Senior Director Compliance and Regulatory
Class II Medical device start-up company. Responsible for the design and implementation of the company quality and assurance systems, including design controls, management controls and CAPA ...
from Dec 2009
Quality Director
1135 Obrien Dr, Menlo Park, CA 94025
Active Implantable Medical device company. Sterile Medical device start-up company. Responsible for the design and implementation of the company quality and assurance systems, including mana...
Nov 2007 — Mar 2009
Quality Director
28515 Westinghouse Pl, Santa Clarita, CA 91355
Active Implantable Medical device company. Led document control, internal audit, CAPA and software QA departments with 27 multilevel reports. Responsible for design and implementation of CAP...
Jun 2006 — Jul 2007
Compliance Director
Medical device/Internet multinational start-up company. Led document control, technical publications, regulatory and software QA departments with 10 multilevel reports. Responsible for desig...
Mar 2005 — Jun 2006
Quality Systems Director
Philips Medical Systems, 2002-2005. Nuclear medicine division of a worldwide medical device company. Managed quality systems, document control, training and multi disciplinary department of ...
Jul 2002 — Mar 2005
Quality and Regulatory Manager
Responsible for all quality and regulatory functions at a e-health startup. Successfully achieved CE Mark approval for lung function monitor in 3 months.
1998 — 2000
Quality Supervisor
Responsible for device testing, audit, CAPA, investigations, complaint handling. Small office of a large multinational company, which was acquired by Roche.
1992 — 1998
Education
Occupations
Executive
Vice President
Senior Director
Sales Specialist
Supplier
Chief Executive
Senior Manager
Operations Manager
Services Professional
Sales Representative
Skills
Iso 13485
Fda
Capa
Quality System
Medical Devices
Validation
Quality Assurance
Design Control
Iso 14971
Cross Functional Team Leadership
Product Development
Manufacturing
21 Cfr Part 11
Iso
Gmp
Quality Management
Regulatory Requirements
Start Ups
V&V
Change Control
Software Documentation
Process Improvement
Regulatory Affairs
Quality Auditing
Document Management
Supplier Quality
Auditing
Ce Marking
Biotechnology
Root Cause Analysis
Fmea
Sop
Continuous Improvement
21 Cfr
Medical Device Directive
Complaint Management
Risk Management
FAQs about Cynthia Merrell
What is the main profession of Cynthia Merrell?
Cynthia is a Vice President Quality and Regulatory.
What jobs is Cynthia proficient at at?
Cynthia Merrell is a professional such jobs as Executive and Vice President.
Where is Cynthia Merrell located?
The professional is located in San Francisco, California.
What is Cynthia's email?
Cynthia's email is cm**@vitalconnect.com and cm**@eneura.com.
Where did Cynthia Merrell work?
Cynthia worked at Vital Connect, Inc., Eneura.
Where has Cynthia Merrell studied?
Cynthia studied at the University of California, Berkeley from 1984 to 1987.
What is the industry that Cynthia Merrell is connected to?
This professional works in Medical Devices industry.
What are professional skills of Cynthia Merrell?
Cynthia has the following skills: Iso 13485, Fda, Capa, Quality System, Medical Devices, Validation, Quality Assurance, Design Control, Iso 14971, and Cross Functional Team Leadership.