For over five years Wendy Jones worked in different jobs. Recently, this professional worked as a Associate Director, Regulatory Affairs in Merz Pharmaceuticals enhancing knowledge. This person graduated from Virginia Polytechnic Institute and State University in 1997 where this expert received all the skills. You can find this professional in Greensboro, North Carolina, where he lives nowadays. Connexy has all the data you need to contact Wendy Jones, such as Wendy Jones's number or email address. Feel free to send the request to get more data.
Name variants:
Gwendolen Jones
Contact Information
Last Update
Jul 17, 2022
Email
wj**@merzusa.com
Location
Greensboro, NC
Company
Workplace
Associate Director, Regulatory Affairs
Greensboro, NC
Industry
Pharmaceuticals, Mfg Pharmaceutical Preparations
Colleagues
Work History
Education
Occupations
Executive
Deputy Director
IT Professional
Software Tester
Deputy Manager
Chief Executive
Computer Specialist
Skills
Regulatory Affairs
Pharmaceutical Industry
Quality Assurance
Fda
Regulatory Submissions
Clinical Development
Microbiology
Clinical Trials
Medical Devices
Ind
Biotechnology
Validation
Cross Functional Team Leadership
Sop
Pharmaceutical Sales
Cro
Drug Development
FAQs about Wendy Jones
What's the main profession of Wendy Jones?
This professional's job is Regulatory Affairs, Pharma and Bio and Device
What jobs is Wendy Jones a professional at?
Wendy Jones is a professional such jobs as Executive and Deputy Director.
Where does Wendy Jones live?
Greensboro, North Carolina is the place where Wendy Jones currently lives
What is Wendy's email?
The expert's email is wj**@merzusa.com.
How many companies did Wendy Jones work at?
The professional worked at four jobs.
What education does Wendy Jones have?
Wendy studied at the Virginia Polytechnic Institute and State University from 1993 to 1997.
Are there any industries, that Wendy Jones is connected to?
This professional works in Pharmaceuticals industry.
Are there any skills Wendy Jones has?
Wendy Jones has such skills as Regulatory Affairs, Pharmaceutical Industry, Quality Assurance, Fda, Regulatory Submissions, Clinical Development, Microbiology, and Clinical Trials.