| Resume alert | Resumes 1 - 10 of 311 |
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
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
Remediation Admin Training Specialist
Tinton Falls, NJ
... review training administration procedures to ensure alignment with current site initiatives, regulatory body requirements (FDA, DEKRA, and AATB) and Global Corporate training procedures Develop criteria to evaluate the effectiveness of training ... - Mar 25
... review training administration procedures to ensure alignment with current site initiatives, regulatory body requirements (FDA, DEKRA, and AATB) and Global Corporate training procedures Develop criteria to evaluate the effectiveness of training ... - Mar 25
Quality Assurance Project Management
North Brunswick, NJ
... Document Management System), SAP(System Applications products in Data Processing) - Provide all necessary documents to FDA, visitors and auditors by putting uncontrolled copies stamp - To maintain all inventories required for documentation. ... - Mar 17
... Document Management System), SAP(System Applications products in Data Processing) - Provide all necessary documents to FDA, visitors and auditors by putting uncontrolled copies stamp - To maintain all inventories required for documentation. ... - Mar 17
Project Management Business Analyst
East Brunswick, NJ
... • Conducted assays and test methods according to 21 CFR and FDA guidelines, including ELISA, BCA (colorimetric assay), LAL endotoxin, SDS-PAGE, and cell culture technique TLR-5 assay (in training). BRISTOL MYERS SQUIBB, Plainsboro, NJ 2004 - 2009 ... - Feb 28
... • Conducted assays and test methods according to 21 CFR and FDA guidelines, including ELISA, BCA (colorimetric assay), LAL endotoxin, SDS-PAGE, and cell culture technique TLR-5 assay (in training). BRISTOL MYERS SQUIBB, Plainsboro, NJ 2004 - 2009 ... - Feb 28
Quality analyst
Lakewood, NJ, 08701
... College Computer science Professional Experience 2022/01 – 2024/01 Quality Analyst -Batch Specialist Life Science Labs •Conducted batches reconciliation, involving precise math calculations to ensure adherence to GMP regulations and FDA guidance. ... - Feb 28
... College Computer science Professional Experience 2022/01 – 2024/01 Quality Analyst -Batch Specialist Life Science Labs •Conducted batches reconciliation, involving precise math calculations to ensure adherence to GMP regulations and FDA guidance. ... - Feb 28
Raw Materials Quality Control
Marlboro, NJ
... Work in heavily FDA regulated cGMP environment and follow lab procedures. Performing adjustment to the in-process batches by calculations when there is out of specification result. Maintain accurate documentation of test results. Enter test results ... - Feb 24
... Work in heavily FDA regulated cGMP environment and follow lab procedures. Performing adjustment to the in-process batches by calculations when there is out of specification result. Maintain accurate documentation of test results. Enter test results ... - Feb 24
Quality Assurance Control/Production Management
Parlin, NJ
... * Reviewed and approved Batch documentations for FDA regulated products. * Document control coordinator for the organization, keeping track of procedures and their lifecycle, issue new procedures and archive old when no longer needed. * Setup ... - Feb 06
... * Reviewed and approved Batch documentations for FDA regulated products. * Document control coordinator for the organization, keeping track of procedures and their lifecycle, issue new procedures and archive old when no longer needed. * Setup ... - Feb 06
Quality Control Product Development
Toms River, NJ
... Contributed to the successful development and FDA clearance of innovative medical devices, including the Connective Tissue Wrap and Placental Extracellular Matrix Osteoconductive Properties. Bioinformatics Programmer CHOP Jan 2022 – Mar 2023 ... - Feb 05
... Contributed to the successful development and FDA clearance of innovative medical devices, including the Connective Tissue Wrap and Placental Extracellular Matrix Osteoconductive Properties. Bioinformatics Programmer CHOP Jan 2022 – Mar 2023 ... - Feb 05