Post Job Free

FDA resumes in Livonia, MI

Sign in
Search for: Jobs   Resumes


distance:
Resume alert Resumes 51 - 60 of 203

Manager Plant

Livonia, MI
... Responsible for the training and monitoring of up to 20 employees for Current Good Manufacturing Practices while monitoring daily quality related items as specified to meet FDA and DOT compliance requirements. Achieved 100% documented accuracy on ... - 2020 Apr 25

Quality / Supplier Quality Engineer

Warren, MI, 48088
... Philips voluntarily shut down production after FDA violation findings. SPQ packages (depending on risk level) contain first article, certs (material, RoHS), GR&R study, special process validation, control plan & FMEA. Daily status meetings to ... - 2020 Apr 09

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

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

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

Employee Relations Sales

Roseville, MI
... Maintained a quality operation in compliance with FDA, OSHA, and other regulatory agencies no observations in last 2 years from any regulatory agency. Strong employee relations resulted in turnover rate at less than fourteen percent (14%). Financial ... - 2020 Feb 03

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

Engineer Medical

Rochester, MI
... Race Engines Medical Device Process Validation WORK HISTORY: ROMD– Rochester Hills, MI December 2018 – Present Manufacturing Engineer Maintain a quality plan and initiate changes in compliance with FDA regulations for medical device manufacturing. ... - 2020 Jan 06

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

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
Previous 3 4 5 6 7 8 9 Next