Michael Bouchon

Associate Director, Regulatory Affairs

Michael Bouchon is a high-skilled expert, working in Lundbeck on the position of Senior Manager, Regulatory Strategy since 2014. Michael has earned professional experience in more than five positions at various companies. Michael Bouchon went to the University of South Carolina and got education from 2009 to 2010. Chicago, Illinois is the area, where this person was known to live. Michael Bouchon's phone number and email can be accessed through this website by request.
Name variants:
Mikael Bouchon, Mychael Bouchon, Mike Bouchon, Mikey Bouchon, Mick Bouchon, Mickey Bouchon, Micky Bouchon, Michl Bouchon, Mischa Bouchon
Last updated Jun 04, 2024

Contact Information

Last Update
Jul 6, 2022
Email
mi**@gmail.com
Location
Chicago, IL
Company

Workplace

Lundbeck
Senior Manager, Regulatory Strategy

Industry

Pharmaceuticals

Work History

Senior Manager, Regulatory Strategy

Manage the implementation of regulatory strategies to ensure the successful clinical development and regulatory approval of prescription drugs. Work across functional areas to ensure that gl...
Jun 2014 — Oct 2017

Associate Director, Regulatory Affairs

Baltimore, MD
Responsible for oversight of the company's Regulatory system, including management of US Regulatory Strategy and Operations. Collaborate with Executive Management and the R&D team to optimiz...
from Oct 2017

Manager, Quality and Regulatory Operations

3530 Toringdon Way SUITE 200, Charlotte, NC 28277
Responsible for life-cycle management of company NDA and IND applications, implementation of company Quality Management System, enrollment in State and Federal licensing programs, co-hosting...
Feb 2012 — Jun 2014

Drug Development and Operations Associate

3530 Toringdon Way SUITE 200, Charlotte, NC 28277
Responsible for the support of many functions across the breadth of the business such as the acquisition and renewal of all required pharmaceutical state-specific licensures and preparation ...
Nov 2010 — Feb 2012

Drug Development Intern

3530 Toringdon Way SUITE 200, Charlotte, NC 28277
Supported Regulatory Affairs in generation and organization of FDA documents and correspondence. Conducted research to support the analysis and review of ongoing clinical trials. Supported Q...
May 2010 — Nov 2010

Education

Occupations

Executive
Deputy Director
Senior Manager
Scientist
Biotechnology Professional
Deputy Manager
Chief Executive
Operations Manager
Biologist
Biological Scientist

Skills

Regulatory Affairs
Clinical Trials
Fda
Quality Assurance
Drug Development
Capa
Quality System
Pharmaceutical Industry
Pharmaceutics
Gcp
Ind
Biotechnology
Pharmacovigilance
Ich Gcp
Sop
U.s. Food and Drug Administration
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