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Product and Process Documentation: Develop and Maintain QMS documents to describe and standardize factory operations; document SOPs for new products or processes to ensure factory readiness; maintain the accuracy and currency of SOPs to reduce cycle time and improve quality.
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Handle Quality Management System (QMS) floor training using Floor Training Tracker. Organize and maintain the supporting organizational structure in the Employee Training Database (employees, roles and associated QMS training requirements) to reflect the quality training requirements of the organization.
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Convert contract documents, proposals and statements of work into work instructions and operating procedures; submit ISO-compliant work instructions and standard operating procedure documents to the Quality Management System (QMS.
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As the Quality Manager, you will oversee quality and maintenance for the site, ensuring that processes needed for the Quality Management System (QMS) are established, implemented and maintained.
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Lean/Six Sigma Black Belt designation. Experience with BI software such as Tableau, Power BI, Data Studio, etc. As the Industrial Engineer, you will be responsible for identifying facility design and personnel requirements to help keep our operations running smoothly.
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Responsible for assessing corporate conformance to the Quality Management System (QMS) Develop, implement, and manage Key Performance Indicators to measure QMS and continuous improvement in the company.
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Experience supporting enterprise software deployments and laboratory/manufacturing equipment and instruments (such as HPLC, MES, ERP, DMS, QMS, etc.) Partner with Regulatory Affairs, Manufacturing, Development, Marketing as well as Corporate Quality on customer projects, regulatory submissions, and harmonization of PPL Group’s Global Quality standards across PPL Group sites.
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Tracks and trends test results and non-conformances using spreadsheets, Product Lifecycle Management (PLM), or Quality Management Systems (QMS) as determined by current process. Product Lifecycle Management, Food Science, Microbiology, Chemistry, Organic, Product Quality.
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Assist in the setup, management, and maintenance of the regulatory information management system (RIMS) and support the Quality function with the implementation of a new quality management system (QMS.
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Regularly report the Area's QMS implementation and audit resolution strategies to the Regional Quality Director. Identify QMS related needs of local Project Managers and leadership and communicate to the Quality Office.
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Perform MES/SAP functions to comply with all QMS requirements. We're in 97% of American homes, and as the leading food and beverage company, our goals are to continue to deliver quality food and beverage products, strengthen our local communities, and reduce our environmental and climate impact.
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Ensure that process techniques are in alignment with Paumac QMS Goals and quality policy. Works on current production work to develop process improvements for efficiency, ergonomics, safety, and part quality.
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Provides QMS Operations related support to all CGMP departments. Experience with Quality System elements for CAPA, Non-Conforming Reports (NCRs) and Deviations. The Quality Analyst I performing quality control (QC) inspection and disposition of materials and products according to specifications.
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The ideal candidate will have a deep understanding of the medical device industry as it pertains to managing and improving a medical device QMS. This person will own the QMS throughout the product life cycle, during agency audits, and the assure the IRRAS Class I measure & sterile, Class IIb electro-mechanical and sterile, and Class III sterile medical devices are held to the highest quality standards.
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Ensure Quality Management Reviews are conducted periodically and report on the quality performance using KPI’s that measure QMS and regulatory compliance and drive improvement. The Product Quality Validation Lead will support tech transfer and validation activities and is a critical part of the global quality organization.
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