Caa Marie Dorat

Owner

Bd
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 Connexy on demand.
Name variants:
Caa Dorat

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Contact Information

Last Update
Jul 9, 2022
Location
San Diego, CA
Company
BD

Workplace

BD
Senior Auditing and Quality Systems Spec Iii - Consultant

Franklin Lakes, NJ

Industry

Medical Devices

Work History

Senior Auditing and Quality Systems Spec Iii - Consultant

Bd
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

Qa Specialist

10210 Genetic Center Dr, San Diego, CA 92121
2006 — 2007

Pfizer Ra Consultant

1235 Rte 1 south, Edison, NJ
2005 — 2006

Regualtory Affairs

1 Dag Hammarskjold Plz, New York, NY 10017
2001 — 2003

Training

1998 — 2001

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.
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