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This role reports directly to the VP of Mortgage Lending and will be responsible for oversight, continuous improvement, and optimization of: real estate post-closing functions, compliance, secondary pricing and rate setting strategies, quality control and origination system administration.
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Coordinates TPM related programs such as product transfers, continuous improvement initiatives, material changes, validation of new manufacturing process, etc., providing oversight and guidance to Supply Chain, Quality, and Regulatory functions.
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JOB PURPOSE: The Senior Packaging Engineer is responsible for project management of packaging initiatives on cross-functional teams that support Brand Marketing new product development and continuous quality and cost improvement projects.
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Supports and maintains all policies of the company including but not limited to ISO/BRC Standards, Health and Safety Requirements, Continuous Improvement, and standard work procedures. Vacation Time Personal Days for Perfect Attendance Additional Benefits: Steel toe boot reimbursement Safety Prescription Glasses reimbursement Uniforms provided at no cost for the employee Purpose: Maintain, repair, and troubleshoot plastic injection molds in order to meet production requirements and molded part quality.
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Contributes to team, company and QMS goals by initiating continuous improvement, accomplishing related results as required and working effectively with other employees and departments. Proven track record of hands-on problem solving and driving continuous quality improvements within a manufacturing environment.
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We value innovation and ingenuity, and we are eager to welcome a talented CNC Machinist who can contribute to our continuous improvement efforts. Job DescriptionJob Overview:As a CNC Machinist, you will play a pivotal role in our manufacturing process, utilizing your exceptional programming skills to create accurate and high-quality parts.
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The Quality Inspector will perform the described quality activities throughout the manufacturing plant as necessary and on a daily basis. About the job 2nd Shift Quality Inspector.
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A key part of the role will be managing the TPM relationship and leading or attending the majority of calls between Abbott and the TPMs. This role will be the key relationship manager between CMI and the TPMs. This role will partner with Engineering and Quality to solve various technical, or quality challenges related to the TPM.
$95,000 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The incumbent oversees the effective integration and continuous improvement of processes and systems to meet MTC’s current and future business goals. Participate in the development, implementation, and monitoring of the department's performance standards, utilizing quality improvement methodologies to refine procedures & policies as required.
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Participate in Corrective and Preventive Action (CAPA) plan actions as means of continuous improvement. Provide quality support to laboratory material receipt, controlled substance program, pest control, calibration, stability, and other laboratory needs.
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Drive continuous improvement in the QMS System (SharePoint). Maintain dealer quality records in warranty system. product/process improvement, commitment to continual departmentimprovement.
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Support and maintain all policies of the company including but not limited to ISO/BRC Standards, Health and Safety Requirements, Continuous Improvement, and standard work procedures. The Quality Assurance Specialist manages the inspection and release of incoming materials, COA/COC process, and Hold for Inspection (HFI) process and supports Document Control process.
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Apply continuous improvement methods such as lean manufacturing to enhance manufacturing quality, reliability, or cost-effectiveness. Effective communicator at all levels; excellent written, oral, and interpersonal communication and presentation skills Experience with pharmaceutical and/or device quality and compliance management systems, desired.
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JOB SUMMARY: Schedules, plans, and coordinates compliance audits and quality systems assessments ensuring compliance with corporate and regulatory provisions of the Quality System. Experience with pharmaceutical and/or device quality and compliance management systems, desired.
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Drives continuous improvement through the R&D Quality Plan process. In collaboration with applicable GXP RDQA Leaders, lead, develop and implement routine and QA oversight strategies relating to R&D business stakeholders including but not limited to Pharmacovigilance and Patient Safety, Regulatory Affairs and Medical Affairs to ensure optimal QA oversight and continuous improvement.
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quality continuous improvement jobs in Green Oaks, IL
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