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We develop drug-delivery systems that are targeted, innovative, environmentally sustainable, and enhance the value of the therapy to the patient and health care system, in order to help patients improve their quality of life and empower them to take control of their disease.
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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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Establishes partnerships and works with Change Control, Quality Engineer team members, and other cross functional managers/supervisors and development engineers/teams to ensure that controlled documents being revised contain the correct information per process/product specifications.
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Reviews and inputs quality control and patient results into the electronic medical records system in a timely manner so clinicians and patients get their results as quickly a possible.
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CommunicationsResponsible for management and quality control of high-level email account for faculty. Calendar ManagementDevelops and maintains administrative support system for complex faculty calendaring and travel planning for faculty.
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As part of the String Team, the Material Control Specialist will work closely with engineering, property management, quality assurance and shipping logistics. They will also be expected to work directly as part of the engineering string team and perform integration and test of the hardware and software of the state-of-the-art AN/TPY-2 radar system.
$48 - $58 an hourExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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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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Facilitate a robust and efficient Quality System including site change control and deviation process. Implement, support, and oversee a document control system, including document review, approval, release, and archiving activities.
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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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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.
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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.
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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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Job Title: Quality Control Inspector I. Basic understanding of Good Manufacturing Practices (GMP) and Quality System Regulations (QSR) Assist Quality Engineering with process and product validation testing.
ExpandApply 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
quality control system jobs in Burlington, MA
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