Resumes
Resumes
![Scott Weit Photo 1 Scott Weit Photo 1](/img/not-found.png)
Vice President Of Quality
View pageLocation:
14 Florys Mill Rd, Flemington, NJ 08822
Industry:
Biotechnology
Work:
Humacyte
Vice President of Quality
Takeda Pharmaceuticals Apr 2019 - Jul 2019
Senior Director, Quality, External Supply Small Molecules and Oncology at Takeda
Takeda Pharmaceuticals Jan 8, 2019 - Apr 2019
Head of Analytical Technology and Knowledge Management
Shire Feb 2018 - Jan 2019
Head of Analytical Technology and Knowledge Management
Shire Jul 2015 - Jan 2018
Head of Analytical Technology
Vice President of Quality
Takeda Pharmaceuticals Apr 2019 - Jul 2019
Senior Director, Quality, External Supply Small Molecules and Oncology at Takeda
Takeda Pharmaceuticals Jan 8, 2019 - Apr 2019
Head of Analytical Technology and Knowledge Management
Shire Feb 2018 - Jan 2019
Head of Analytical Technology and Knowledge Management
Shire Jul 2015 - Jan 2018
Head of Analytical Technology
Education:
The University of Georgia 1986 - 1990
Doctorates, Doctor of Philosophy, Philosophy, Chemistry Shippensburg University of Pennsylvania 1982 - 1986
Bachelors, Bachelor of Science, Chemistry Warwick Senior High School
University of Georgia
Doctorates, Doctor of Philosophy, Philosophy, Chemistry Shippensburg University of Pennsylvania 1982 - 1986
Bachelors, Bachelor of Science, Chemistry Warwick Senior High School
University of Georgia
Skills:
Gmp
Pharmaceutical Industry
Fda
Validation
Quality Assurance
Analytical Chemistry
Technology Transfer
Drug Development
Glp
Sop
R&D
Quality Control
Biotechnology
V&V
Capa
U.s. Food and Drug Administration
Quality System
Pharmaceutics
Clinical Trials
Computer System Validation
Hplc
Manufacturing
Leadership
Management
Biopharmaceuticals
Formulation
Laboratory
Product Development
21 Cfr Part 11
Standard Operating Procedure
Change Control
Regulatory Submissions
Chromatography
Cross Functional Team Leadership
High Performance Liquid Chromatography
Integration
Lims
Strategic Planning
Budgets
Characterization
Clinical Development
Commercialization
Gxp
Good Laboratory Practice
Laboratory Information Management System
Research and Development
R
Regulatory Affairs
Pharmaceutical Industry
Fda
Validation
Quality Assurance
Analytical Chemistry
Technology Transfer
Drug Development
Glp
Sop
R&D
Quality Control
Biotechnology
V&V
Capa
U.s. Food and Drug Administration
Quality System
Pharmaceutics
Clinical Trials
Computer System Validation
Hplc
Manufacturing
Leadership
Management
Biopharmaceuticals
Formulation
Laboratory
Product Development
21 Cfr Part 11
Standard Operating Procedure
Change Control
Regulatory Submissions
Chromatography
Cross Functional Team Leadership
High Performance Liquid Chromatography
Integration
Lims
Strategic Planning
Budgets
Characterization
Clinical Development
Commercialization
Gxp
Good Laboratory Practice
Laboratory Information Management System
Research and Development
R
Regulatory Affairs
Languages:
English
![Scott Weit Photo 2 Scott Weit Photo 2](/img/not-found.png)
Scott Weit
View pageLocation:
Lititz, PA