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In person or Remote (East Coast with initial training onsite at Bridgewater, NJ and few days for the first few months)DutiesThe CMC Regulatory Technical Writer II authors high quality Module and regulatory submissions for both development and post-approval dossiers, change controls and technical reports.
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Good fit for anyone with sales experience in the water quality/water filtration industry. Conduct territory site visits offering our water quality, conditioning, and filtration solutions.
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Manage critical metrics for the Branchburg Quality organization, including Quality Index, Site Business Review, Quality Systems Management Review, and Post Market Surveillance Review.
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The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. A background of pharmaceutical manufacturing or quality control/quality assurance is a plus.
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Financial Crimes Compliance Quality and Model Risk Analyst! The successful candidate will be responsible for ensuring the efficacy and accuracy of our financial crimes compliance software, as well as other quality assurance tasks related to compliance.
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Experience with Veeva (Quality Docs, QMS and Training modules) a plus. Global Pharmaceutical company, with US HQ in Central New Jersey, focused in Metabolics, Endocrinology and Oncology is expandingLooking for a strong Quality Assurance Manager for the entire North American manufacturing and quality organization.
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Position Overview: The Supplier Quality Engineer - Medical Device will be responsible for ensuring the quality of materials and components received from suppliers for use in the production of medical devices.
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Posting Summary Rutgers, The State University of New Jersey, is seeking a Program Development Analyst – Quality Improvement, Assessment, and Accreditation Specialist for the Office of Education at the Robert Wood Johnson Medical School.
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14+ years of overall experience in Quality Engineering and Assurance working in the Consulting environment. Extensive experience to QA automation to various tools like Selenium, Tosca, Rest Assured, etc.
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Lead Lean or Six Sigma projects to streamline processes, reduce waste, and improve overall quality. Monitor Supplier Quality and performance. Foster a culture of quality and continuous improvement within the organization.
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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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On-Board Services is hiring a Quality Control Chemist in New Brunswick, NJ! per hourLength of Assignment: year with a possibility of extension The Quality Control Chemist for the drug product testing team reports to the Finished Product/Stability Supervisor.
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Must understand and apply cGMP requirements applicable to quality control laboratory. Perform testing using HPLC, UPLC, GC, IR, UV, Malvern Mastersizer, XRD, Dissolution, Karl-Fischer titrator, analytical balances, and other instruments as required.
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Position requires on-site presence at companies' HQ Essential Duties and Responsibilities Conducting Training: Developing and conducting training programs for personnel on GMP and GDP requirements, quality systems, and relevant procedures to ensure understanding and compliance throughout the organization.
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Developing and Maintaining Quality Systems: Establishing and maintaining comprehensive quality systems in compliance with GMP and GDP regulations. Continuous Improvement Initiatives: Leading or participating in continuous improvement initiatives to enhance the effectiveness and efficiency of quality systems and processes, driving a culture of quality and excellence within the organization.
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Title: quality Company: Direct Line Global in Bridgewater, NJ
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