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The Sr. Associate Compliance provides scientific support in the root cause analysis and closure of OOS investigations, OOT investigations and product quality complaints; ensures compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP) and Quality Management System standards, compiles monthly Quality metrics for internal and corporate review, and analyzes trends to implement corrective and preventive actions to mitigate adverse trends.
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Knowledge of vendor/supplier management Program Working knowledge of Trackwise to handle electronic Quality Manage System (eQMS) data, EDMS for SOPs and LMS for trainings. Ensure compliance of establish Quality Management System (QMS) and in compliance with corporate requirements and all applicable FDA Part , Part /, Part , ISO and Canadian Medical Devices Regulations (CMDR SOR/-), EU Medical Device Regulation.
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Experience with DeltaV Process Control System and SAP in a cGMP environment is desirable. Actively leads a bulk chemical manufacturing production line working with other shift supervisors to ensure consistency across all shiftsDevelops weekly production schedule by partnering with Production Planning, Supply Chain, Quality, and Product Management teams.
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In this role, you will be responsible for developing, implementing, and maintaining comprehensive record retention systems, implementing the electronic file system, ensuring accuracy, quality and integrity of all company documents, providing training for all employes on the record system, reviewing and updating documents for maintenance and quality control, and perform other tasks and duties as assigned.
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You will own and process Quality Management Standard documents - including ISO forms, Return Material Authorizations (RMA) and quality control action plans. Within the ERP system (Epicor) you will capture of all supporting documentation for orders and portfolios included but not limited to freight invoices, inventory management documents and coordinate product receipt and release from location warehouse.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Strong knowledge of Trackwise to handle electronic Quality Manage System (eQMS) data. Manage electronic Quality Management System (TrackWise) Preferably knowledge to handle SAP, EDMS, LMS, Master Control etc.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Implement electronic Quality Systems, such as eQMS, EDMS, and LMS, providing procedures and training for employees to effectively use the electronic Quality Systems. Develop presentation monthly for QRB meeting based on eQMS, Quality Matrix and Monthly Quality investigation Board (QIB) meeting.
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Thorough understanding of key supporting quality systems including change control, deviation / non-conformance, and CAPA. Expertise in root cause analysis. System owner of the site’s validation and engineering program; drafts, defines, and revises submission packets, procedures to ensure compliance to cGMP, GLP, FDA and worldwide regulations.
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Ensures Quality Control of the exams by using the PACS system. Licensed by the Commonwealth of Massachusetts’ Department of Public Health: Radiation Control Program in Radiography.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Work closely with the Business, Global Financial Services, Treasury, Tax, and Financial Reporting and Planning functions to ensure the quality, accuracy and consistency of the financial data reported in the general ledger and consolidation system.
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Serve as control account manager and provide effective Earned Value Management System (EVMS) analysis and management. Facilitate compliance with the Raytheon Quality Management System while driving continuous improvement.
$118,000 - $246,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Who will be providing scientific support in the root cause analysis and closure of OOS investigations, OOT investigations and product quality complaints; ensures compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP) and Quality Management System standards, compiles monthly Quality metrics for internal and corporate review, and analyzes trends to implement corrective and preventive actions to mitigate adverse trends.
$100,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Job Summary: The Inventory Control Coordinator is responsible for ensuring quality and accuracy of all inventory in the DC by executing cycle counts, completing physical inventories, conducting food safety audits and supporting Quality department initiatives.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Initiates product quality complaints in our Quality Management System (QMS). Other functional responsibilities may include authoring and revising Quality System Documentation and trending and evaluating Product Quality.
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Food Safety & Quality System knowledge to produce safe quality food, acting as SQF Practitioner. Administers the implementation of food safety and quality (FSQ) programs including hazard analysis and critical control point (HACCP) program, sanitation standard operating procedures, pest control, good manufacturing practices, approved supplier program, foreign material control, plant sanitation, chemical control, product quality assurance, FSQ customer complaints, and food defense and security.
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quality control system jobs in Tewksbury, MA
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