Directory
>
Paul Talierco
Paul Talierco
Vice President, Head Regulatory Affairs CMC | Ironwood Pharmaceuticals
Allentown, Pennsylvania, United States
Paul Talierco
Summary
Paul Talierco is a seasoned Regulatory CMC Executive with extensive expertise in the pharmaceutical industry, particularly in regulatory affairs related to chemistry, manufacturing, and quality. With a robust background in analytical chemistry and biopharmaceuticals, he has a proven track record of leading cross-functional teams and developing effective regulatory strategies. Throughout his career, Paul has been instrumental in managing complex regulatory submissions and ensuring compliance with FDA regulations. His leadership style emphasizes mentorship and team development, fostering a culture of continuous improvement. Paul has successfully navigated the regulatory landscape for multiple high-profile products, including vaccines and monoclonal antibodies. His strategic thinking and problem-solving skills have consistently driven organizational efficiency and product quality enhancements. Beyond his technical acumen, Paul is recognized for his ability to build strong relationships with stakeholders and business partners. He is committed to advancing the field of regulatory affairs through innovation and collaborative practices.
Paul Talierco
Work Experience
Vice President, Head Regulatory Affairs CMC at
Ironwood Pharmaceuticals
June 2023 - Present
Executive Director, Regulatory Affairs CMC at
Global Blood Therapeutics, Inc.
March 2022 - May 2023
Senior Director, Regulatory Affairs CMC at
Global Blood Therapeutics, Inc.
September 2020 - March 2022
Director at
Global Regulatory Writing & Consulting, Inc.
December 2019 - September 2020
Executive Director at
Merck
December 2018 - November 2019
Director Vaccines RA CMC at
Merck
December 2016 - December 2018
Director, Biopharm CMC Regulatory Affairs at
GSK
March 2015 - December 2016
Associate Director, Biopharm CMC Regulatory Affairs at
Glaxosmithkline
January 2011 - March 2015
Associate Director, Regulatory Affairs CMC at
ImClone Systems, a wholly-owned subsidiary of Eli Lilly and Company
January 2010 - January 2011
Deputy Director, Industrial CMC Compliance at
Sanofi
January 2006 - January 2010
Senior Specialist, Global Manufacturing Compliance/Reg CMC at
Pfizer, Inc.
January 2004 - January 2006
Senior Supervisor at
Merck
January 1999 - January 2004
Supervising Chemist at
West Pharmaceutical Services
January 1996 - January 1999
Paul Talierco
Education
Regulatory Affairs Professionals Society, Rac (Us)
January 2006 - January 2006
Georgia Southern University, Ms
January 1995 - January 1996
wheeling university, Bs
January 1990 - January 1994
Frequently Asked Questions about Paul Talierco
What is Paul Talierco email address?
Paul Talierco's primary email address is *********@gbt.com. To view the full verified email and additional contact details, sign up for free with Muraena.
What company does Paul Talierco work for?
Paul Talierco is a Vice President, Head Regulatory Affairs CMC at Ironwood Pharmaceuticals, a company specializing in Commercial physical research.
Where Paul Talierco graduated from?
Paul Talierco holds a degree in Regulatory Affairs from Regulatory Affairs Professionals Society.
How can I directly contact Paul Talierco?
To contact Paul Talierco directly, you can use the email address *********@gbt.com. Complete contact information is available upon registration with Muraena.
Who is Paul Talierco?
Paul Talierco is a seasoned Regulatory CMC Executive with extensive expertise in the pharmaceutical industry, particularly in regulatory affairs related to chemistry, manufacturing, and quality. With a robust background in analytical chemistry and biopharmaceuticals, he has a proven track record of leading cross-functional teams and developing effective regulatory strategies. Throughout his career, Paul has been instrumental in managing complex regulatory submissions and ensuring compliance with FDA regulations. His leadership style emphasizes mentorship and team development, fostering a culture of continuous improvement. Paul has successfully navigated the regulatory landscape for multiple high-profile products, including vaccines and monoclonal antibodies. His strategic thinking and problem-solving skills have consistently driven organizational efficiency and product quality enhancements. Beyond his technical acumen, Paul is recognized for his ability to build strong relationships with stakeholders and business partners. He is committed to advancing the field of regulatory affairs through innovation and collaborative practices.
Paul`s contact details
*********@gbt.com
*************@vectivbio.com
*********@ironwoodpharma.com
Colleagues
Vice President, Head of Data Science
Vice President, Global Patient Safety
Vice President Manufacturing and Technical Operations
Vice-President, Corporate Strategy
Vice President of Brand Management
Vice President, Corporate Controller, Principal Accounting Officer, & Treasurer
Member Board of Directors
Chief Financial Officer
VP Product Promotion & Communication
Vice President Global Medical and Scientific Affairs