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Resume alert |
Resumes 11 - 20 of 403 |
Malvern, PA
... • Reviewed lab personnel notebooks for compliance with FDA regulations and internal SOPs. • Recipient of an Above & Beyond Award. EDUCATION MS, Biochemistry, East China University of Science and Technology, Shanghai, China Thesis: Chemical ...
- Mar 05
West Chester, PA
... Experience within a regulated industry (medical devices desirable, along with knowledge of Product Lifecycle Management, FDA Quality System Regulations and ISO 13485) Responsible for tracking of CR/CN in Windchill with Approval from stakeholders ...
- Mar 04
Philadelphia, PA
... provided Quality oversight of internal and external clinical trial activities, related records, and processes to assure management in accordance with FDA regulations, ICH-GCP, SOPs and all other applicable regulations and assisted with other tasks ...
- Feb 26
Havertown, PA
... ability to talk with individuals at all levels • Very knowledgeable with CRO, Clinical trial processes, HIPAA and other myriad FDA regulations and compliances Professional Experience Diagnostic Solutions Laboratory 2013-2022 Director, New Business ...
- Feb 22
Pennsauken, NJ
... lung, and gastric cancers across 15 sites in the United States from start-up activities including feasibility, final protocol, FDA follow-up, study and site contracts and budgets, master ICF development and approval, oversight of site ICF ...
- Feb 18
New Castle, DE
... and in compliance with federal and state regulations and guidelines including FDA, EPA, DOT, OSHA, & DEA Ensures accurate, up-to-date records of inventory through SAP and daily operations, completes necessary forms and data entry is completed. ...
- Feb 14
Philadelphia, PA
... Key Achievements: • Secured FDA approval for five items within a 24-month timeframe. • Introduced high-speed, needle-free injection systems at US military bases. • Positioned the company as a frontrunner in global health endeavors targeting ...
- Feb 11
Philadelphia, PA
... Knowledge of FDA and HIPPA regulations, medical terminology, laboratory testing procedures and equipment. Familiar with GLP and GCP environment. A highly motivated person with strong analytical and organizational skills. A dedicated team player also ...
- Feb 06
Philadelphia, PA
... Comply to all SOP, cGMP, SAP, AND FDA standards. October 2004- March 2018 Animas Corporation of Johnson & Johnson West Chester, PA Served in several employment capacities and have demonstrated Johnson & Johnson Credo values while fulfilling numerous ...
- Feb 05
Hockessin, DE
... Subject matter expert (SME), oncology, hematology, cardio-metabolic disease, reproductive care, and genetics in communications with the Food and Drug Administration (FDA) and Advisory Board. Used knowledge in CART-T Cell immunotherapy, stem cell ...
- Jan 23