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Resume alert |
Resumes 41 - 50 of 151 |
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
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
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
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
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
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
Colchester, ON, Canada
... Knowledge in FDA systems for overseas shipments including use of broker systems and courier companies Assess and resolve customer complaints and keeping professional records Accommodations and financial coordination for international trade shows and ...
- 2019 Apr 25
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
Redford, MI
... and total protein to determine if donor is suitable to donate Performs annual training and recertification for CLIA and FDA regulations Educates donor about risks of donating plasma Educates donor on steps to take to ensure a successful donation ...
- 2019 Apr 04
Lincoln Park, MI, 48146
... Maintain FDA Releases from the custom brokers as well as good communication and tracking during load transit, during and after crossing the border; Aid in commercialization of the product in the USA. Communication with sales team in regards to ...
- 2018 Nov 25