Sales Administration Manager jobs in the Quality Assurance & Safety category and Consumer Packaged Goods Manufacturing industry in Illinois

QUALITY ASSURANCE MANAGER -FOOD INDUSTRY LEADER – GREAT OPPORTUNITY One of the category leaders in the food industry with over $1B in sales and growing consistently seeks a Quality Assurance / Food Safety Manager for a facility with rapidly expanding production capacity and demand. POSITION SUMMARY: In this role you will be in charge of quality audits, perform pre-operational inspection of equipme...
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Description New Position- Because of growth Medline Industries, Inc. has an immediate opening for a Sr. Regulatory Affairs Manager located in the Mundelein, IL facility. This position will focus on U.S. regulatory affairs as it relates to medical device, OTC drug, and other product development with an emphasis on 510(k) submissions, plus unique device identification, clinical study and testing rev...
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Site Overview Custom Division's Danville, IL contract manufacturing plant is located conveniently in Danville with 300,000 square feet of production space. The facility runs 24 hours at 5 days a week and is registered and compliant with the FDA, EPA, & cGMP. The facility is capable of manufacturing quality products in the following: steel or aluminum aerosol cans, bag on valve, and liquid filling ...
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Site Overview Custom Division's Danville, IL contract manufacturing plant is located conveniently in Danville with 300,000 square feet of production space. The facility runs 24 hours at 5 days a week and is registered and compliant with the FDA, EPA, & cGMP. The facility is capable of manufacturing quality products in the following: steel or aluminum aerosol cans, bag on valve, and liquid filling ...
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Description Medline Industries has an immediate opening for Associate QA Specialist-Supplier Quality position, located in Mundelein, IL headquarters. The Associate QA Specialist will be responsible for quality assurance activities related to the Supplier Quality group within the QA/RA Division. The position will be responsible for maintaining design control files and device master records for FDA ...
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