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Resume alert |
Resumes 1 - 10 of 710 |
Kendall Park, NJ
... EDUCATION Master’s of Science in Regulatory Affairs & Health Policy MCPHS University Boston, MA Dec 2017 GPA:3.91/4.00 Bachelor’s of Science in Pharmacy Veer Narmad South Gujarat University India May 2005 GPA: 3.25/4.00 EDUCATION DETAILS • FDA ...
- Apr 29
Plainsboro, NJ
... sales and marketing and opinion leaders to develop and implement products labelling strategy to meet the requirements of the FDA and other regulatory agencies to achieve enhanced FDA’s agreements to company’s approval desires based on products ...
- Apr 21
Lawrence Township, NJ
... Maintained rigorous compliance in clinical trial operations, meticulously ensuring that all patient-related content aligned with FDA regulations and Bristol-Myers Squibb (BMS) guidelines. As well as ensuring that all CMC practices were updated ...
- Apr 18
Piscataway, NJ
... scales for weight verification, and calculators for accurate counts Strict adherence to SOP's which are in compliance with the FDA, CGMP, ISO regulations and company health and safety procedures This includes line clearances, set up of batch records ...
- Apr 14
Lawrenceville, NJ
... Skills Used Documentation Skills, Analyzing Information, Chemistry Techniques, Informing Others, FDA Health Regulations, Creating a Safe, Effective Environment, Infection Control, Training Management, Lab Environment, Clinical Lab Testing, ...
- Apr 13
Plainsboro, NJ
... Implemented new processes that maintain a highly FDA regulated site and a network security design to ensure adherence of HIPPA regulations. Redesigned computer network. Effectively executed new network policies and procedures. Responsible for ...
- Apr 04
East Brunswick, NJ, 08816
... Supported technology transfer related activities from development to launch for drug products (DPs) at BMS manufacturing sites (or external manufacturing) according to BMS directives, ICH, FDA and regulatory guidelines. Performed physical testing on ...
- Apr 03
Belle Mead, NJ
... • Expert knowledge of Global and FDA Regulations supporting the submission of Adverse Events for Post- marketing and Clinical Trials drugs. • Understanding of ICH guidelines on PV and application of guidelines detailed in FDA 21 CFR Part 11, ...
- Mar 29
Iselin, NJ, 07067
... Good Automated Manufacturing Practices (GAMP 5) risk-based approach Provided Validation services in achieving the 21 CFR PART 11 (Electronic Records & Signatures) compliance to assure successful data quality and data integrity to, and FDA challenge. ...
- Mar 28
Bridgewater, NJ
... Developed online Learning Management System (LMS) for certification process training and to meet FDA / compliance requirements. Provided guidance on change management methodology and related communications for stakeholder and user clarity. Ricoh ...
- Mar 26