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                        Jobs at Medline Industries, Inc. in Pleasant Prairie, Wisconsin

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                        Description We have a Senior Systems Administrator role in which you will primarily be responsible for implementing, monitoring, troubleshooting, maintaining, upgrading, and securing all Windows-based systems. This includes staying on top of the latest technologies and understanding where they can fit into Medline's infrastructure. Also, implementation of systems involves working with the applicat...
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                        Description Medline has an immediate opening for a Business Process Analyst. Under the general direction of Finance Operations Director, the Business Process Analyst is instrumental in the identification, verification, design, and successful implementation of system enhancements and business process improvements for key Finance processes involving hundreds of thousands of transactions annually. Th...
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                        Description Because of growth Medline Industries, Inc. has an immediate opening for an International Regulatory Affairs Specialist - located in the Mundelein, IL facility. This position will focus on international regulatory affairs as it relates to medical device product development and various international submissions, research, review, medical device manufacturing, and regulatory aspects of ve...
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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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                        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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