Tony Freeman

Associate Director, Global Project Management

Tony Freeman is a qualified expert, that works in Jazz Pharmaceuticals as a Associate Director, Global Project Management from 2018. This expert has earned professional experience in more than nine positions at various companies. Tony Freeman went to the Tulane University - A.b. Freeman School of Business and got education from 2006 to 2008. This person has such qualifications as Project Management Professional (Pmp)® and Project Management Institute (Pmi). Cheltenham, Pennsylvania is the area, where this expert was known to settle. The professional's e-mail and phone can be easily accessed through this website on demand.
Name variants:
Anthony Freeman, Shelton Freeman, Antoinette Freeman, Antonia Freeman
Last updated Jun 23, 2024

Contact Information

Last Update
Jul 1, 2022
Email
to**@jazzpharma.com, tf**@msn.com
Location
Cheltenham, PA
Company
Jazz Pharmaceuticals

Workplace

Associate Director, Global Project Management

Work History

Associate Director, Global Project Management

from Aug 2018

Project and Portfolio Management

Nov 2017 — Jul 2018

Associate Director, Global Project Management

2000 Galloping Hill Rd, Kenilworth, NJ 07033
This site is intended only for residents of the United States and its territories. Merck is known as MSD outside the United States and Canada. Today's Merck is a global healthcare leader wor...
May 1, 2015 — Nov 2017

Global Project and Portfolio Manager

20 Kingsbridge Rd, Piscataway, NJ 08854
Aug 2014 — May 2015

Global Project Manager

Aug 2013 — Mar 2014

Project Manager

1100 Orthodox St, Philadelphia, PA 19124
May 2006 — Apr 2013

Professional Sales Representative

Apr 1999 — Apr 2005

Senior Research Associate

Dec 1996 — Apr 1999

Chemist

New York, NY
Oct 1993 — Dec 1996

Occupations

Executive
Deputy Director
Deputy Manager
Chief Executive

Skills

Gmp
Pharmaceutical Sales
Regulatory Affairs
Sop
Pharmaceutical Industry
Technology Transfer
Hplc
Project Management
Analytical Chemistry
Validation
Chromatography
Lims
21 Cfr Part 11
V&V
Gcp
Regulatory Submissions
Fda
R&D
Glp
Quality Assurance
Capa
Quality System
Pharmaceutics
Chemistry
Change Control
Drug Development
Computer System Validation
Clinical Development
Gxp
Cro
Clinical Trials
Biotechnology
Regulatory Requirements
Lifesciences
Biopharmaceuticals
Vaccines
Oncology
Drug Discovery
Ind
Medical Devices
Laboratory
Medical Writing
Quality Control
Cleaning Validation
Life Sciences
Standard Operating Procedure
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