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Paul Talierco

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Paul Talierco

Vice President, Head Regulatory Affairs CMC | Ironwood Pharmaceuticals

Allentown, Pennsylvania, United States

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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.

General

Specialist

Technical Background

Leadership Experience

Long-Term Tenure

Professional interests

Emerging Technologies

Leadership Development

Sustainability

Organisational experience

Corporate Experience

Paul Talierco

Work Experience

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Vice President, Head Regulatory Affairs CMC at

Ironwood Pharmaceuticals

June 2023 - Present

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Executive Director, Regulatory Affairs CMC at

Global Blood Therapeutics, Inc.

March 2022 - May 2023

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Senior Director, Regulatory Affairs CMC at

Global Blood Therapeutics, Inc.

September 2020 - March 2022

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Director at

Global Regulatory Writing & Consulting, Inc.

December 2019 - September 2020

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Executive Director at

Merck

December 2018 - November 2019

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Director Vaccines RA CMC at

Merck

December 2016 - December 2018

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Director, Biopharm CMC Regulatory Affairs at

GSK

March 2015 - December 2016

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Associate Director, Biopharm CMC Regulatory Affairs at

Glaxosmithkline

January 2011 - March 2015

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Associate Director, Regulatory Affairs CMC at

ImClone Systems, a wholly-owned subsidiary of Eli Lilly and Company

January 2010 - January 2011

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Deputy Director, Industrial CMC Compliance at

Sanofi

January 2006 - January 2010

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Senior Specialist, Global Manufacturing Compliance/Reg CMC at

Pfizer, Inc.

January 2004 - January 2006

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Senior Supervisor at

Merck

January 1999 - January 2004

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Supervising Chemist at

West Pharmaceutical Services

January 1996 - January 1999

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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

mail

*********@gbt.com

*************@vectivbio.com

*********@ironwoodpharma.com

Colleagues

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Thomas Wright

Vice President Manufacturing and Technical Operations

Harriet Winter

Vice-President, Corporate Strategy

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Tammi Gaskins

Vice President of Brand Management

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Ron Silver

Vice President, Corporate Controller, Principal Accounting Officer, & Treasurer

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Thomas Mccourt

Member Board of Directors

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Sravan Emany

Chief Financial Officer

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Sharon Debacco

VP Product Promotion & Communication

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Mena Boules Md

Vice President Global Medical and Scientific Affairs

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