Caa Marie Dorat is a high-skilled professional, who works in Bd main office of which is in 179. on the position of Senior Auditing and Quality Systems Spec Iii - Consultant since 2019. Caa Marie Dorat gained professional experience in more than 22 positions at various companies. Caa Marie Dorat went to the New York University and got education from 1984 to 1989. This expert has such professional qualifications as Certified Apostille Agent, Notary Public, and State of California. San Diego, California is the city, where this person was lastly known to settle. This person's email address and phone are easily accessed through SoftwareOfficial on demand.
Name variants:
Caa Dorat
Last updated Jun 17, 2024
Workplace
Senior Auditing and Quality Systems Spec Iii - Consultant
Franklin Lakes, NJ
Industry
Medical Devices
Colleagues
Work History
Senior Auditing and Quality Systems Spec Iii - Consultant
1 Becton Dr, Franklin Lakes, NJ 07417
May 2019 — Nov 2019
Clinical Trial Auditor
100 Cummings Ctr SUITE 206L, Beverly, MA 01915
Audit clinical trial sites compliance to VICH GL9 (GCP) regulations (17 sites)
Audit CRO oversite of clinical trial sites & data management
from Nov 2019
Senior Auditor
125 north Acacia Ave SUITE 101, Solana Beach, CA 92075
from May 2018
Sw Qa Manager
190 north Milwaukee St, Milwaukee, WI 53202
Software QA Manager - QMS Development & Training
May 2017 — Mar 2018
Principal Quality Compliance Analysts and Capa Specialist
710 Medtronic Pkwy, Fridley, MN 55432
CAPA Remediation; CAPA Training & Internal Audits
May 2016 — Feb 2017
Regulatory and Quality Specialist
8999 Biolegend Way, San Diego, CA
RA/QA Compliance for global BioLegend commercial sites
Develop/implement QMS
Implement eQMS for global sites
Maintain FDA/EU compliance program
International product registrations
Comp...
Aug 2015 — May 2016
Gxp Webinar Presenter
New York, NY
Webinar presenter for the following courses:
FDA vs EU Inspections
GCP
Auditing 101
International Product Registration – Lessons Learned
Sep 2013 — 2016
360 Expert
13801 Burnet Rd SUITE 100, Austin, TX 78758
Life Science Change Management Configuration & development of 360Factors Life Sciences module.
May 2014 — Feb 2015
Senior Validation Consultant
1100 Campus Rd, Princeton, NJ
Develop, implement Site Validation Master Program
Jul 2014 — Dec 2014
Managing Partner
San Diego, CA
Regulatory/Quality Compliance/Auditing
GxP Compliance Training
International product registration
All apostille and/or embassy legalizations usually completed within 48 - 72 hours. Exped...
from May 2014
Gxp Webinar Presenter
38780 Tyson Ln APARTMENT 210, Fremont, CA 94536
Webinar presenter for the following courses:
FDA vs EU Inspections
GCP
Auditing 101
from Feb 2014
Ra and Qa Consultant
Develop Quality System procedures
Develop HIPAA/HITECH procedures
Develop Clinical Trial specific procedures
Provide QMS training
2013 — 2014
Senior Qa Compliance Consultant
65 Hayden Ave, Lexington, MA 02421
Develop clinical auditing program
Manage cGMP/Clinical audits
o Manage CROs & Audit consultants
Perform Clinical/cGMP/GLP/PV audits
Develop Quality & GCP training program
o Provide com...
Jan 2013 — Dec 2013
Quality Systems Consultant
La Jolla, CA
Develop company Quality System Standard Operating Procedures Regulatory Compliance
Aug 2012 — Mar 2013
Regulatory Affairs Rebranding Specialist
100 Abbott Park Rd, North Chicago, IL 60064
Specialist in International Registration of Medical Device & IVDs
Compiling registration documentation and technical files for rebranding project for international and domestic permits and...
May 2010 — Dec 2011
Owner
Notary Public/Certified Loan Signing Agent/Certified Apostille Agent.- specializing in International medical device registrations. Let me reduce your medical international registration time ...
from Aug 2011
Regulatory Compliance and Quality Systems Auditor
California
Sep 2008 — Jul 2010
Quality Assurance Supervisor
4 Chrysler, Irvine, CA 92618
Supervisor QA /Document Control
Implement Master Control EDC system
Provide MC training
Assess for ISO 17025 certification
Perform Internal Audits
2008 — 2008
Education
Occupations
Executive
Owner
Counselor
Accountant
Auditor
Chief Revenue Officer
Chief Executive
Advisor
Skills
Fda
Quality System
Quality Assurance
Medical Devices
Regulatory Affairs
Validation
Quality Auditing
Biotechnology
Gmp
Management
Iso 13485
Pharmaceutical Industry
Capa
Change Control
Process Improvement
Training
Clinical Trials
Gcp
Quality Management
Cross Functional Team Leadership
Auditing
21 Cfr Part 11
Sop
Glp
R&D
Document Management
Quality Control
V&V
Lifesciences
Software Documentation
Notary Public
Clinical Research
Iso
Manufacturing
Employee Training
Iso 9000
Hardware Diagnostics
Six Sigma
Root Cause Analysis
Data Management
Oncology
Product Launch
Pharmaceutics
Staffing Services
Temporary Placement
Cro
Process Engineering
Market Development
Internet Recruiting
Executive Management
FAQs about Caa Marie Dorat
What's the main profession of Caa Marie Dorat?
Caa Marie Dorat is a Owner.
What jobs is Caa proficient at at?
Caa Marie Dorat is a professional Executive and Owner jobs.
Where does Caa Marie Dorat currently live?
San Diego, California is the place where Caa Marie Dorat lives
Where did Caa Marie Dorat work?
Caa Marie Dorat worked at Bd, Oxford Global Resources.
Where has Caa Marie Dorat studied?
Caa studied at the New York University from 1984 to 1989.
What are the certifications of Caa Marie Dorat?
The professional received the following certifications: Certified Apostille Agent, Notary Public, and State of California.
What languages does Caa Marie Dorat speak?
Caa Marie Dorat speaks English, French, and Spanish.
Are there any professional industries Caa Marie Dorat works in?
This person works in Medical Devices industry.