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Works with the Manager of Regulatory Compliance to ensure all settings that are on the DPH license comply with TJC standards and the CMS COPs Supports Medical Staff credentialing as requested Supports the SMG Quality Department with Culture of Safety implementation and continuing education.
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The Quality Assurance Specialist II will provide onsite intermediate-level, hands-on support from a regulated systems perspective in a GxP laboratory services, repository, and kitting production environment.
$50,000 - $86,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A minimum of five (5) years of Manufacturing Engineering or Supplier Quality Engineering experience, preferably in an Engineered-to-Order facility. A Bachelors Degree in Quality Engineering, Manufacturing Engineering, Mechanical Engineering, or similar technical discipline is required.
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Quality Engineer Kelly Services is currently seeking a Quality Engineer for one of our top clients in Raynham, MA. The Laboratory Quality Engineer is responsible for the completion of quality deliverables within the laboratory including Audit, CAPA, and Nonconformance investigation and management to meet quality performance measures established by the business.
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Quality Engineering/Process Excellence/Lean experience. Knowledge of the QSR, Design Controls, and ISO quality requirements. The Quality Engineer I will be able to communicate effectively at all levels within Quality as well as cross functionally with departments such as R&D, Regulatory, Manufacturing, Medical Affairs and Marketing.
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About the position:As a member of the CDC Warehouse Organization, you will be part of Quality Care team responsible for maintaining the CDC inventory integrity, researching order shortages, item discrepancies and inventory discrepancies and assisting the Sales team in ticket maintenance when necessary.
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Support the continuous improvement of quality system processes through the development of Statistical Process Control Plans and subsequent collection, evaluation and reporting of performance to established control limits.
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Responsibilities include conducting in-process analytical testing, performing organoleptic and visual inspections, auditing cook stations and packaging lines to ensure adherence to HACCP food safety protocols, initiating corrective actions for any food safety or quality issues, conducting equipment environmental swabbing, maintaining effective communication across production and management levels, and completing all daily paperwork with accuracy and detail.
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Job DescriptionSUMMARY:Reporting to the Quality Manager, the Quality Inspector works under the Quality performing Quality Control inspection on composite tilesESSENTIAL DUTIES AND RESPONSIBILITIESInspects incoming materials and parts visually and mechanically from outside vendors to ensure conformance to specifications and certifications.
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The ideal candidate should demonstrate proficient experience with quality management concepts and Project Management including but not limited to supplier quality, eQMS, risk assessment, process qualification, process controls, root cause investigations, CAPA, and continuous improvement.
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The Quality Control Analyst is responsible for reviewing Medical Disability Examination (“MDE”) reports and Disability Benefits Questionnaires (“DBQs”) generated by medical providers for veterans evaluated on behalf of the Department of Veterans Affairs (the “VA.
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We are working with a client this is looking for a qualified Quality Assurance Manager to join their team with comprehensive knowledge of manufacturing processes and ISO9001 Our client builds the world's most powerful, combat systems for survivable naval ships and defense technology solutions that safeguard our warfighter on seas, sky, land, space & cyber.
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The Senior Director Quality Engineering will be accountable for the development, execution, and delivery of quality strategies for DPS TECA and Mitek Sports Medicine lifecycle management (LCM) and new product introduction (NPI) engineering activities.
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Provide leadership in all areas of the Quality System, including, but not limited to Corrective & Preventive Actions, Risk Management, Complaints, Post Market Surveillance, Nonconforming Materials, etc.
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This position will lead the implementation of Quality processes and Inspection Readiness Activities, assist with the management of the audit program and partner with key cross-functional groups (e.g., Clinical Operations, Regulatory, Biometrics, Pharmacovigilance) to ensure compliance of RRD's activities for continuous process improvement.
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Title: quality Company: Proactive Strategies in Easton, MA
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