Benjamin Johns Email & Phone Number
Director of Global Regulatory Affairs @ Taiho Oncology, Inc.
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Benjamin Johns Location
- Warminster, PA, US
Benjamin Johns Work
- Director of Global Regulatory Affairs @ (June 2019 - Present)
- Associate Director of Regulatory Affairs @ (June 2017 - May 2019)
- Regulatory Affairs Strategist @ (October 2014 - June 2017)
- Consultant, Regulatory Affairs - CMC @ (September 2012 - September 2014)
- Senior Technical CMC Strategist @ (January 2011 - August 2012)
- Regulatory Affairs Consultant @ Pharma Regulatory Consultants (November 2008 - December 2010)
- Associate Director, Product Development @ MedPointe Pharmaceuticals (September 2003 - October 2008)
- Senior Scientist and Team leader @ (November 1999 - September 2003)
- Senior Scientist @ Sandoz (Eon Labs) (November 1996 - October 1999)
- Manufacturing Supervisor @ (July 1993 - August 1996)
Benjamin Johns Education
- Trident University International
Doctorate in Healthcare Administration (PhD)
2004-2010 - St. John's University
Master of Science - MS (Industrial Pharmacy)
- St. John's University
Master of Science (Pharmaceutics and Drug Design)
Benjamin Johns Skills
- Communication
- Manufacturing
- Global Regulatory Compliance
- Research and Development (R&D)
- Briefing
- Chemistry, Manufacturing, and Controls (CMC)
- Regulatory Policy
- Pharmaceutical Manufacturing
- Regulatory Intelligence
- Manufacturing Operations
- FDA GMP
- Regulatory Risk
- Regulatory Affairs
- FDA
- Pharmaceutical Industry
- Technology Transfer
- Regulatory Submissions
- CMC Regulatory Affairs
- Formulation
- Drug Development
- Pharmaceutics
- Quality Assurance
- CRO
- Validation
- Change Control
- IND
- CMC
- Cross-functional Team Leadership
- ANDA
- Biotechnology
- GMP
- Lifesciences
- Pharmacovigilance
- Clinical Trials
- Regulatory Requirements
- NDA
- Sop
- Clinical Development
- Biopharmaceuticals
- Oncology
- Life Sciences
- Standard Operating Procedure (SOP)
- U.S. Food and Drug Administration (FDA)
- Strategy
- cGMP manufacturing
- Corrective and Preventive Action (CAPA)
- CTA
- New Drug Application (NDA)
- DMF
- Standard Operating Procedure Sop
- Project Management
- Customer Service
- Regulatory
- Social Media
- Research
- u.s. Food and Drug Administration Fda
- Cross Functional Team Leadership
- Leadership
- Biochemistry
- Strategic Planning
- Marketing
- u.s. Food and Drug Administration
- Standard Operating Procedure
Benjamin Johns Summary
- Benjamin Johns, based in Warminster, PA, US, is currently a Director of Global Regulatory Affairs at Taiho Oncology, Inc.. Benjamin Johns brings experience from previous roles at Insud Pharma, Bayer, Merck and Pfizer. Benjamin Johns holds a 2004 - 2010 Doctorate in Healthcare Administration (PhD) @ Trident University International. With a robust skill set that includes Communication, Manufacturing, Global Regulatory Compliance, Research and Development (R&D), Briefing and more. Benjamin Johns has 3 emails and 5 mobile phone numbers on RocketReach.
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Top Taiho Oncology, Inc. Employees
Michael Schick
Chief Business Officer (CBO)
Furlong, PA, US
Christine Guertin
Vice President Regulatory Affairs
Boston, MA, US
Harold Keer
Chief Medical Officer
California, United States
Ed Chapman
Chief Information Officer
Hendersonville, TN, US
Peter Melnyk
President and CEO
Cold Spring Harbor, NY, US
Juliet Agranoff
Chief People Officer
New York, NY, US
Einav Leberknight
Vice President, Clinical Operations
New Jersey, United States
Said Rahal
Vice President-Pharmacovigilance
Berkeley Heights, NJ, US
Kathy Calarco
Senior Vice President of Quality
Philadelphia, PA, US
Mike Mitchell
Vice President, Market Access and Policy
St. Louis, MO, US
Timothy Wert
Vice President, Market Access and Policy
Newtown, PA, US
Elizabeth Calleja
Vice President Clinical Development
New York, NY, US
Nancy Worrell
Vice President, People
California, United States
Masayuki Kanai
Vice President, Precision Medicine
United States
Debbie Bensen-Kennedy
Senior Vice President Medical Affairs
Phoenixville, PA, US
Tim Whitten
CEO
Princeton, NJ, US
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