Resumes
Resumes
![Smita Gadhiya Photo 1 Smita Gadhiya Photo 1](/img/not-found.png)
Senior Manager It Validation
View pageLocation:
Piscataway, NJ
Industry:
Pharmaceuticals
Work:
Taiho Oncology Inc
Senior Manager It Validation
Novartis Sep 2015 - Jun 2018
Project Quality Manager
Impax Laboratories Aug 2014 - Aug 2015
Computer System Validation and Quality Manager
Johnson & Johnson Apr 1, 2012 - Aug 1, 2014
Computer System Quality Validation Manager
Bristol-Myers Squibb May 2009 - Mar 2012
Information Management Quality Assurance Computer System Validation Manager
Senior Manager It Validation
Novartis Sep 2015 - Jun 2018
Project Quality Manager
Impax Laboratories Aug 2014 - Aug 2015
Computer System Validation and Quality Manager
Johnson & Johnson Apr 1, 2012 - Aug 1, 2014
Computer System Quality Validation Manager
Bristol-Myers Squibb May 2009 - Mar 2012
Information Management Quality Assurance Computer System Validation Manager
Education:
Gujarat Uni. School of Sciences 1988 - 1990
Master of Science, Masters, Biotechnology, Microbiology Fatima Convent High School 1974 - 1983
Master of Science, Masters, Biotechnology, Microbiology Fatima Convent High School 1974 - 1983
Skills:
Computer System Validation
21 Cfr Part 11
Validation
Cgmp
Gxp
Sop
Gmp
Lims
Change Control
Capa
Gamp
Fda
Quality Assurance
Quality Systems
Sdlc
Document Management
Medical Devices
Documentation
Compliance
Regulatory Affairs
Documentum
Glp
Auditing
Testing
Business Analysis
Quality Management
Risk Management
Sap
Software Documentation
Quality System
Quality Auditing
Software Quality Control
Pharmaceutical Industry
Quality Control
Regulatory Submissions
Gcp
Biopharmaceuticals
Iso 13485
Trackwise
21 Cfr Part 11
Validation
Cgmp
Gxp
Sop
Gmp
Lims
Change Control
Capa
Gamp
Fda
Quality Assurance
Quality Systems
Sdlc
Document Management
Medical Devices
Documentation
Compliance
Regulatory Affairs
Documentum
Glp
Auditing
Testing
Business Analysis
Quality Management
Risk Management
Sap
Software Documentation
Quality System
Quality Auditing
Software Quality Control
Pharmaceutical Industry
Quality Control
Regulatory Submissions
Gcp
Biopharmaceuticals
Iso 13485
Trackwise