FDA resumes in Elkridge, MD

Hopkins Bayview, MD, 21224
... - Reengineer FDA CDRH core processes w/ Accenture (510K, EUA, PMA, DeNovo PAS/522, Standards Review, Device Shortages, FOIA, External Comms, Q-Sub, BIMO, Recalls, CLIA) to improve decision time (TTD), increase MDUFA IV performance and reduce ... - 2023 Nov 13

Baltimore, MD
... • You will find me well versed in all aspects of food production and catering, including budgeting, FDA guidelines, HACCP certification, menu research and development, purchasing and warehouse organization, inventory control, and personnel ... - 2023 Oct 13

Odenton, MD
... • Work with NCATS and FDA staff to prioritize the development and implementation of features, services and tools on the project’s critical development path. • Model the generation of necessary software and process documentation. • Assess code ... - 2023 Sep 25

Baltimore, MD
... charts and followed testing and inspection procedures · Maintained accurate records and logs in accordance with FDA (Food and Drug Administration), GMPs (Good Manufacturing Practices) and ISO9000 (International Organization for Standardization). ... - 2023 Sep 02

Perry Hall, MD
... Administration (FDA) General administrative activities: including but not limited to, domestic and international travel, set up teleconference, videoconferences, and onsite/off-site meetings, extensive calendar, filing, faxing and mail distribution. ... - 2023 Aug 28

Baltimore, MD
... Select key clients: Absolut, Brand USA, CES, Colorado Tourism, Cruise Lines International Association, Donate Life Maryland, Energy Star, FDA, Harrah's Entertainment, Hershey's Chocolate World, HMSHost, Johns Hopkins University, Lending Tree, ... - 2023 Aug 24

Silver Spring, MD
... Language skills: English (Advanced), French (Intermediate), Tamil (mother tongue) Industry Experience ORISE fellow-Office of Pharmaceutical Quality (OPQ), FDA January 30/2023-Present • Working on a research project focusing on the manufacturing of ... - 2023 Aug 14

Baltimore, MD
... changes for impact on the regulatory status of the product Communicates with regulatory and governmental agencies with supervision Applies FDA regulations to business practices and provides regulatory input, advice, and guidance to design teams. ... - 2023 Jul 31

Maryland
... Write, coordinate, compile, manage and submit Regulatory documents to FDA and other Regulatory Agencies, including International Authorities. Lead auditor for FDA form 482 (form for inspection) and lead meetings with the FDA, answering FDA inspector ... - 2023 Jul 04

Annapolis Junction, MD
... Host and passed al center audits (FDA, PPTA, EAU, KED, Grifols, Internal, AGES) • Train and help develop New Center Managers, assistant managers and all roles in thecenter. • C r e a t e training teams and environments to assistwith training and ... - 2023 Jun 25