Scott Weit Email & Phone Number
Vice President of Quality @ CTI BioPharma
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Scott Weit Location
- Lititz, PA, US
Scott Weit Work
- Vice President of Quality @ (September 2022 - Present)
- Vice President of Quality and Company Compliance Officer @ (September 2019 - May 2022)
- Senior Director, Quality, External Supply Small Molecules and Oncology at Takeda @ (April 2019 - July 2019)
- Head of Analytical Technology and Knowledge Management @ (February 2018 - January 2019)
- Head of Analytical Technology - Outsourced Products Liaison @ (July 2015 - January 2018)
- Senior Scientific Director - Analytical Development - Clinical Product Development Phases I, Ii, Iii @ (November 2009 - June 2015)
- Senior Director Quality Control Services - Clinical Development Phases I and Ii @ (June 2008 - December 2009)
- Worldwide Director Quality Assurance and Analytical Services - Commercial Products @ (January 2007 - June 2008)
- Director, Quality Systems - Commercial Products @ (January 2006 - December 2006)
- Head of Quality, Johnson and Johnson - Merck Joint Venture @ (September 2003 - December 2005)
- Director, New Jersey Quality Services - Consent Decree Rebuild @ (December 2001 - September 2003)
- Director, North American Stability - Drug Product and Api Stability @ (March 1999 - October 2001)
- Director, West Point Quality Operations - Pharmaceutical and Biological Commercial Products @ (January 1995 - February 1999)
- Laboratory Manager, Analytical Methods and Support - Methods Development and Characterization @ (September 1993 - December 1994)
- Laboratory in-Process Testing Manager, Quality Operations @ (October 1991 - August 1993)
- Technical Operations - Senior Chemist and Senior Staff Chemist @ (August 1990 - September 1991)
- Research Assistant and Teaching Assistant @ (June 1986 - August 1990)
Scott Weit Education
- University of Georgia
Doctor Of Philosophy (Philosophy, Chemistry)
1986-1990 - Ship
Bachelor Of Science (Chemistry)
1982-1986
Scott Weit Skills
- GMP
- FDA
- Validation
- Quality Assurance
- Pharmaceutical Industry
- Analytical Chemistry
- R&D
- V&V
- Quality Control
- Drug Development
- Computer System Validation
- Manufacturing
- 21 CFR Part 11
- Biopharmaceuticals
- Biotechnology
- GLP
- Clinical Trials
- Formulation
- HPLC
- Integration
- LIMS
- Laboratory
- Technology Transfer
- Strategic Planning
- SOP
- R
- Product Development
- Pharmaceutics
- Budgets
- CAPA
- Change Control
- Characterization
- Leadership
- Management
- Quality System
- Clinical Development
- Regulatory Submissions
- Commercialization
- Chromatography
- Cross-functional Team Leadership
- GxP
- Regulatory Affairs
- Good Laboratory Practice Glp
- Cross Functional Team
- High Performance Liquid Chromatography Hplc
- Research And Development R&D
- Laboratory Information Management System Lims
- Cross Functional Team Leadership
- U.S. Food And Drug Administration Fda
- Standard Operating Procedure Sop
- Computer System
- Research and Development
- Standard Operating Procedure
- Laboratory Information Management System
- High Performance Liquid Chromatography
- u.s. Food and Drug Administration
- Good Laboratory Practice
Scott Weit Summary
- Scott Weit, based in Lititz, PA, US, is currently a Vice President of Quality at Cti Biopharma. Scott Weit brings experience from previous roles at Humacyte, Takeda Pharmaceuticals and Shire. Scott Weit holds a 1986 - 1990 Doctor Of Philosophy in Philosophy, Chemistry @ University of Georgia. With a robust skill set that includes GMP, FDA, Validation, Quality Assurance, Pharmaceutical Industry and more. Scott Weit has 3 emails and 2 mobile phone numbers on RocketReach.
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