| Resume alert | Resumes 41 - 50 of 180 |
Clinical Research Assistant
Ypsilanti, MI
... federally and industry sponsored •Assists with the preparation of protocols for IRB submission and renewals •Maintains compliance with study protocols •Plans and coordinates audits with project sponsors, including FDA; Responsible for complying with ... - 2020 Jun 20
... federally and industry sponsored •Assists with the preparation of protocols for IRB submission and renewals •Maintains compliance with study protocols •Plans and coordinates audits with project sponsors, including FDA; Responsible for complying with ... - 2020 Jun 20
Engineer Process
Ann Arbor, MI
... compliance with CFR Part 820.30 “Design Controls” o Implement Engineering Change Orders (ECOs) • Lead-process engineer during FDA approval/auditing process • Established and maintained supplier relations including alternate sourcing and issuance of ... - 2020 Jun 19
... compliance with CFR Part 820.30 “Design Controls” o Implement Engineering Change Orders (ECOs) • Lead-process engineer during FDA approval/auditing process • Established and maintained supplier relations including alternate sourcing and issuance of ... - 2020 Jun 19
Technician Service
Warren, MI
... Chicago, IL, 2006 – 2008 (Contract Position) Field Service Biomedical Technician Traveled from state to state to customer sites performing upgrades, major repairs, inspections, and final testing on Baxter medical devices, following FDA procedures. ... - 2020 Jun 08
... Chicago, IL, 2006 – 2008 (Contract Position) Field Service Biomedical Technician Traveled from state to state to customer sites performing upgrades, major repairs, inspections, and final testing on Baxter medical devices, following FDA procedures. ... - 2020 Jun 08
Medical Device
Royal Oak, MI
TANAYA JOSHI adc5r2@r.postjobfree.com +1-313-***-**** Detroit, MI Skills Medical device diagnostics Equipment Troubleshooting & Preventive Maintenance MATLAB & SimBiology Tool Analog Circuit Design ISO 13485 ISO 14971 Regulatory Affairs FDA ... - 2020 May 10
TANAYA JOSHI adc5r2@r.postjobfree.com +1-313-***-**** Detroit, MI Skills Medical device diagnostics Equipment Troubleshooting & Preventive Maintenance MATLAB & SimBiology Tool Analog Circuit Design ISO 13485 ISO 14971 Regulatory Affairs FDA ... - 2020 May 10
Data Analyst
Ann Arbor, MI
... first researcher of the Center for the Assessment of the Public Health Impact of Tobacco Regulations, a part of the NIH and FDA's Tobacco Centers of Regulatory Science · Population Assessment of Tobacco and Health (PATH) study - Longitudinal data ... - 2020 Mar 25
... first researcher of the Center for the Assessment of the Public Health Impact of Tobacco Regulations, a part of the NIH and FDA's Tobacco Centers of Regulatory Science · Population Assessment of Tobacco and Health (PATH) study - Longitudinal data ... - 2020 Mar 25
Machine Operator Power Plant
Detroit, MI
Kenyetta McDaniel *** * *********** *** ** Detroit, MI 48201 adcfqu@r.postjobfree.com 313-***-**** Authorized to work in the US for any employer Work Experience Machine Operator/Material Handler Euclid Manufacturing - Detroit, MI August 2018 to... - 2020 Mar 25
Kenyetta McDaniel *** * *********** *** ** Detroit, MI 48201 adcfqu@r.postjobfree.com 313-***-**** Authorized to work in the US for any employer Work Experience Machine Operator/Material Handler Euclid Manufacturing - Detroit, MI August 2018 to... - 2020 Mar 25
Machine Operator, Customer Service
Detroit, MI, 48206
... Responsible for performing tests on products at various stages of production to ensure that customer specifications are being met and SQF, FDA and USDA standards are followed. Production/Assembly Worker BING STEEL MANUFACTURING, Highland Park, MI 02 ... - 2020 Feb 26
... Responsible for performing tests on products at various stages of production to ensure that customer specifications are being met and SQF, FDA and USDA standards are followed. Production/Assembly Worker BING STEEL MANUFACTURING, Highland Park, MI 02 ... - 2020 Feb 26
Engineer Quality
Farmington, MI
... Audit supplier on ISO 13485, and Work with FDA on Quality Improvement. Eliminated (PPAP ) parts that are obsolescent parts from Supplier base that resulted in a 20% improvement with a cost saving of $ 600K. Streamlined the (PPAP) process by ... - 2020 Jan 28
... Audit supplier on ISO 13485, and Work with FDA on Quality Improvement. Eliminated (PPAP ) parts that are obsolescent parts from Supplier base that resulted in a 20% improvement with a cost saving of $ 600K. Streamlined the (PPAP) process by ... - 2020 Jan 28
Industrial, mechanical, process, quality, AutoCAD, Visio, SAS
Canton, MI, 48188
... Inspection and quality control support of renal concentrates products as per the cGMP and FDA standards. UT Southwestern Medical Center, Dallas, TX June 18 - September 18 Quality Engineer Impacting about 40,000 chronic pain patients of UT health ... - 2019 Sep 13
... Inspection and quality control support of renal concentrates products as per the cGMP and FDA standards. UT Southwestern Medical Center, Dallas, TX June 18 - September 18 Quality Engineer Impacting about 40,000 chronic pain patients of UT health ... - 2019 Sep 13
Web Developer
Westland, MI
... •Guide new product development through the quality system to ensure products are developed in compliances to their procedures and the requirements of the FDA and ISO. Senior Capstone Project: Design of Dimethyl Ether Production (DME). •Designed and ... - 2019 Apr 20
... •Guide new product development through the quality system to ensure products are developed in compliances to their procedures and the requirements of the FDA and ISO. Senior Capstone Project: Design of Dimethyl Ether Production (DME). •Designed and ... - 2019 Apr 20