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Chris Sharpe
Chris Sharpe
VP, Regulatory Affairs | Quell Therapeutics
Chartridge, England, United Kingdom
Chris Sharpe
Summary
Chris Sharpe is a seasoned professional in regulatory affairs with a rich background that spans over 15 years in the pharmaceutical industry. He began his career as a pharmacist before transitioning into regulatory roles, gaining experience as a pharmaceutical assessor at the MHRA and working with major companies like GSK, Wyeth, and Allergan. His leadership skills were honed at Biogen, where he built the regulatory department for the UK and Irish affiliate and later served as a Global Regulatory Lead. Currently, as the VP of Regulatory Affairs at Quell Therapeutics, Chris drives innovative regulatory strategies in the biotechnology sector. His expertise encompasses clinical development, drug formulation, and regulatory submissions, making him a crucial player in advancing therapeutic solutions. Chris's journey reflects a commitment to excellence and a deep understanding of regulatory landscapes, which is essential for navigating the complexities of drug development and compliance.
Chris Sharpe
Work Experience
VP, Regulatory Affairs at
Quell Therapeutics
December 2021 - Present
Head Of Regulatory Affairs at
Quell Therapeutics
September 2019 - December 2021
Global Regulatory Lead at
Biogen
July 2018 - September 2019
Associate Director, Regulatory Affairs, UK and Ireland at
Biogen
July 2015 - July 2018
Director, Regulatory Affairs (EU) at
Kuur Therapeutics
December 2012 - July 2015
EU Regulatory Affairs Senior Manager at
Allergan
January 2012 - December 2012
Regulatory Affairs Manager at
Allergan
November 2010 - December 2011
Pharmaceutical Assessor at
Medicines and Healthcare products Regulatory Agency
February 2009 - November 2010
Regulatory Affairs Officer at
Pfizer
June 2008 - January 2009
Regulatory Executive at
GSK
September 2006 - June 2008
Locum Pharmacist at
LloydsPharmacy
August 2005 - September 2006
Chris Sharpe
Education
University of Nottingham, Master's Degree
January 2000 - January 2004
University of Nottingham, Master's Degree
Frequently Asked Questions about Chris Sharpe
What is Chris Sharpe email address?
Chris Sharpe's primary email address is ********@quell-tx.com. To view the full verified email and additional contact details, sign up for free with Muraena.
What company does Chris Sharpe work for?
Chris Sharpe is a VP, Regulatory Affairs at Quell Therapeutics, a company specializing in Commercial physical research.
Where Chris Sharpe graduated from?
Chris Sharpe holds a degree in Pharmacy from University of Nottingham.
How can I directly contact Chris Sharpe?
To contact Chris Sharpe directly, you can use the email address ********@quell-tx.com. Complete contact information is available upon registration with Muraena.
Who is Chris Sharpe?
Chris Sharpe is a seasoned professional in regulatory affairs with a rich background that spans over 15 years in the pharmaceutical industry. He began his career as a pharmacist before transitioning into regulatory roles, gaining experience as a pharmaceutical assessor at the MHRA and working with major companies like GSK, Wyeth, and Allergan. His leadership skills were honed at Biogen, where he built the regulatory department for the UK and Irish affiliate and later served as a Global Regulatory Lead. Currently, as the VP of Regulatory Affairs at Quell Therapeutics, Chris drives innovative regulatory strategies in the biotechnology sector. His expertise encompasses clinical development, drug formulation, and regulatory submissions, making him a crucial player in advancing therapeutic solutions. Chris's journey reflects a commitment to excellence and a deep understanding of regulatory landscapes, which is essential for navigating the complexities of drug development and compliance.
Chris`s contact details
********@quell-tx.com
Colleagues
Svp Research & Translation
VP clinical operations
Chief Medical Officer