| Resume alert | Resumes 1 - 10 of 730 |
Clinical Research Business Development
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
... 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
Senior Manager / Associate Director
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
... 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
Customer Service Rep
North Plainfield, NJ
... Dayton, NJ • Managed arriving vessels for spice company overseeing and serving as the company’s liaison • Handled the compliance of Customs regulations, in addition to coordinating with FDA and clearing Customs with Brokers • Generated purchase ... - Apr 15
... Dayton, NJ • Managed arriving vessels for spice company overseeing and serving as the company’s liaison • Handled the compliance of Customs regulations, in addition to coordinating with FDA and clearing Customs with Brokers • Generated purchase ... - Apr 15
Medical Courier Pick Up
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
... 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
Medical Assistant Pharmacy Technician
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
... 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
Case Management Customer Service
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
... 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
Formulation/scale up of solid dosage forms
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
... 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
Drug Safety Information Technology
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
... • 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
Business Analyst Change Management
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
... 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
Project Manager Change Management
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
... 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