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Resumes 41 - 50 of 673 |
Chicago, IL
... Food and Drug Administration (FDA)-approved Standard Operating Procedure Manual, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP) and internal company ...
- 2023 Nov 28
Naperville, IL
... Lead, Product Development, Sales and Clinical Trainer • Developed, implemented, and managed alpha and beta testing phases for pre-market clinical evaluation and FDA approval for a remote-site trans-telephonic non-invasive cardiac monitoring device. ...
- 2023 Nov 28
Chicago, IL
... 6/2013 to 11/2016 Hologic Sr Interaction Designer Sunnyvale, CA Responsible for user research, interaction design, usability testing, and leading junior designers for a generative, web-based, FDA-approved, 3D mammography application for radiologists ...
- 2023 Nov 25
Western Springs, IL
... LUKE’S, Chicago, IL (1996-1997) Unit Service Manager Managed three units and 40 union employees Responsible for all non-clinical unit services, including FDA, JCAHO compliance ADVOCATE HOME HEALTHCARE DIVISION, Bridgeview, IL (1993-1995) ...
- 2023 Nov 24
Bartlett, IL, 60103
... production control, raw material planning, inventory control, shipping and receiving •Utilized applicable standard operating procedures (SOPs) and FDA regulations while working in a current good manufacturing practice (cGMP) laboratory SDI, Inc. ...
- 2023 Nov 16
Lake Zurich, IL
... Medical Device Testing: IoT testing where medical equipment is controlled by iOS/Android App, Cloud data logs analysis and equipment data analysis, participated in FDA iOS and Android 510K releases. Also involved in device testing via mobile ...
- 2023 Nov 14
Palatine, IL
... Performed quantitative chemical analysis and compiled data in compliance with corporate, OSHA, EPA, and FDA standards Tested samples of products at various stages of production processes and compiled statistical data to determine and maintain ...
- 2023 Nov 13
Elk Grove Village, IL
... functional teams to verify presented material complies with regulatory guidelines set forth by the Food & Drug Administration (FDA) Interpreted FDA guidance documents and warning letters to understand what is and what is not allowed in advertisement ...
- 2023 Nov 09
Bartlett, IL
... •Maintain quality system requirements in accordance with ISO 13485 and FDA 21 CFR 820. •Maintain safe work environment and follow GMP policies. •Develop technical expertise, support 5S, lean six sigma and continuous improvement projects to increase ...
- 2023 Nov 09
Buffalo Grove, IL, 60089
... Since Siemens Healthcare was FDA regulated, their suppliers were required to have an ISO level quality system. Siemens Healthcare’s initial audit in 2007 identified 26 major findings. Within 6 months, I developed a comprehensive quality system that ...
- 2023 Oct 29