Resumes
Resumes
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Associate Director Quality Assurance
View pageLocation:
52 Rockledge Dr, Pleasant Valley, NY 12569
Industry:
Pharmaceuticals
Work:
Johnson & Johnson Mar 2011 - 2015
Program Manager, Global System Quality Assurance
Janssen Research and Development Mar 2011 - 2015
Associate Director Quality Assurance
Johnson & Johnson Jun 2009 - Mar 2011
Senior Specialist
Johnson & Johnson Mar 2007 - Jun 2009
Senior Specialist, Therapeutic Area Quality Assurance
Johnson & Johnson Feb 2004 - Mar 2007
Senior Associate
Program Manager, Global System Quality Assurance
Janssen Research and Development Mar 2011 - 2015
Associate Director Quality Assurance
Johnson & Johnson Jun 2009 - Mar 2011
Senior Specialist
Johnson & Johnson Mar 2007 - Jun 2009
Senior Specialist, Therapeutic Area Quality Assurance
Johnson & Johnson Feb 2004 - Mar 2007
Senior Associate
Education:
Virginia Commonwealth University 1996 - 1996
Bachelors, Bachelor of Science University of Bombay 1988 - 1988
Bachelors, Bachelor of Science, Pharmacy
Bachelors, Bachelor of Science University of Bombay 1988 - 1988
Bachelors, Bachelor of Science, Pharmacy
Skills:
Quality Assurance
Pharmaceutical Industry
Sop
Regulatory Affairs
Fda
Capa
Gcp
Validation
Clinical Trials
Gmp
Quality Auditing
Clinical Research
Pharmacovigilance
Clinical Development
Standard Operating Procedure
Computer System Validation
U.s. Food and Drug Administration
21 Cfr Part 11
Regulatory Requirements
Good Clinical Practice
Biotechnology
Quality Management
Auditing
Powerpoint
Research
Program Management
Quality System
Ctms
Glp
Software Documentation
Microsoft Word
Oncology
Regulatory Submissions
Quality Control
Pharmaceutics
Life Sciences
Medical Devices
Drug Development
Gxp
Change Control
Clinical
Compliance
Pharmaceuticals
Quality Systems
Clinical Trial Management
Word
Cro
Immunology
Microbiology
Pharmaceutical Industry
Sop
Regulatory Affairs
Fda
Capa
Gcp
Validation
Clinical Trials
Gmp
Quality Auditing
Clinical Research
Pharmacovigilance
Clinical Development
Standard Operating Procedure
Computer System Validation
U.s. Food and Drug Administration
21 Cfr Part 11
Regulatory Requirements
Good Clinical Practice
Biotechnology
Quality Management
Auditing
Powerpoint
Research
Program Management
Quality System
Ctms
Glp
Software Documentation
Microsoft Word
Oncology
Regulatory Submissions
Quality Control
Pharmaceutics
Life Sciences
Medical Devices
Drug Development
Gxp
Change Control
Clinical
Compliance
Pharmaceuticals
Quality Systems
Clinical Trial Management
Word
Cro
Immunology
Microbiology
Languages:
English
Hindi
Marathi
Spanish
Hindi
Marathi
Spanish
Certifications:
Ascp
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