Resumes
Resumes
Independent Consultant
View pageLocation:
226 Winged Foot Dr, Blue Bell, PA 19422
Industry:
Pharmaceuticals
Work:
Keystone Biologics Regulatory Consulting
Independent Consultant
Accord Healthcare
Executive Vice President, Global Regulatory Affairs
Dr. Reddy's Laboratories Feb 2014 - Oct 2018
Vice President, Regulatory Affairs at Dr Reddy's Labs
Gsk Aug 2010 - Dec 2013
Vice President, Global Regulatory Affairs - Biopharmaceuticals and Vaccines
Temple University College of Pharmacy Aug 2010 - Dec 2013
Adjunct Professor, Qa and Ra Graduate Program
Independent Consultant
Accord Healthcare
Executive Vice President, Global Regulatory Affairs
Dr. Reddy's Laboratories Feb 2014 - Oct 2018
Vice President, Regulatory Affairs at Dr Reddy's Labs
Gsk Aug 2010 - Dec 2013
Vice President, Global Regulatory Affairs - Biopharmaceuticals and Vaccines
Temple University College of Pharmacy Aug 2010 - Dec 2013
Adjunct Professor, Qa and Ra Graduate Program
Education:
The Ohio State University 1983 - 1985
Doctorates, Doctor of Philosophy, Microbiology The Ohio State University 1981 - 1983
Master of Science, Masters, Microbiology Lafayette College 1977 - 1981
Bachelors, Bachelor of Arts, Biology
Doctorates, Doctor of Philosophy, Microbiology The Ohio State University 1981 - 1983
Master of Science, Masters, Microbiology Lafayette College 1977 - 1981
Bachelors, Bachelor of Arts, Biology
Skills:
Vaccines
Regulatory Affairs
Biopharmaceuticals
Biotechnology
Pharmaceutical Industry
Oncology
Clinical Development
Cmc
Regulatory Submissions
Clinical Research
Drug Development
Monoclonal Antibodies
Technology Transfer
Fda
Gmp
Clinical Trials
Cancer
Analytical Chemistry
Drug Discovery
Infectious Diseases
Ind
Glp
Leadership
Pharmaceutics
Sop
Commercialization
Validation
V&V
Pharmacology
Regulatory Requirements
Quality System
Regulations
Gcp
21 Cfr Part 11
Change Control
Capa
Medical Devices
Product Development
Therapeutic Areas
Ctms
Immunology
Biosimilars
Biomarkers
Medical Affairs
Medical Writing
R&D
Market Access
Lifesciences
Project Management
Cro
Regulatory Affairs
Biopharmaceuticals
Biotechnology
Pharmaceutical Industry
Oncology
Clinical Development
Cmc
Regulatory Submissions
Clinical Research
Drug Development
Monoclonal Antibodies
Technology Transfer
Fda
Gmp
Clinical Trials
Cancer
Analytical Chemistry
Drug Discovery
Infectious Diseases
Ind
Glp
Leadership
Pharmaceutics
Sop
Commercialization
Validation
V&V
Pharmacology
Regulatory Requirements
Quality System
Regulations
Gcp
21 Cfr Part 11
Change Control
Capa
Medical Devices
Product Development
Therapeutic Areas
Ctms
Immunology
Biosimilars
Biomarkers
Medical Affairs
Medical Writing
R&D
Market Access
Lifesciences
Project Management
Cro