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The Sr. Director, Quality Technical Operations, Cell Therapy Manufacturing is responsible for leading the day-to-day quality review and approval of investigations, CAPA, Change Controls with associated documents and the oversight of the Quality Engineering team responsible for qualifications and validations of computerized systems, software, enterprise systems, equipment, methods, and manufacturing processes.
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Training and professional skill development will be provided for the various aspects of the position, with opportunity for growth into a project management position. My Client , a highly successful and growing full service environmental consulting firm specializing in contaminated property investigation/cleanup/redevelopment and LSRP services, is seeking a project-level Geologist or Environmental Scientist with a minimum two years of experience to join our team and provide technical support on a wide range of investigation and remediation projects.
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Proven experience in using source code tools (Git, Bitbucket) and project management tools such as JIRA, ADO. Infrastructure as Code (IaC): Utilize infrastructure as code principles to automate the provisioning and management of Azure resources using tools like ARM templates, Terraform, or Azure Resource Manager.
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The Technical Writer and Document Specialist (TW/DS) will sit within the Cell Therapy Development (CTD) Development Operations and Services (DO&S) Portfolio Management Office (PMO). Partner with SME organizations to identify source documents and negotiate delivery of approved technical documents in accordance with project timelines and aligned with CTD requirements and regulatory strategy.
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Strong business andor technical background in the areas of Master Data Management Data Quality Data Governance Data Integration ETL SoA and Data Security. Deliver endtoend master data management projects for our customers that includes but not limited to Designing data model MDM Hub configuration.
$120,000 - $140,000 a yearFull-timeExpandUpdated Yesterday - UpvoteDownvoteShare Job
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Collaborate with cross-functional teams, including CATD teams, CMC, Analytical Science and Technology (AS&T), Quality Control, Regulatory Affairs, and Project Management, to ensure alignment and successful execution of automation projects.
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The Administrative Assistant in the Quality Improvement department facilitates, organizes, and assists the division of Clinical Transformation/Integration, that includes: Quality, Medical Staff, Care Management/transition,physician liaison, and Infection Prevention to include but not limited to: scheduling meetings, minute taking, correspondence, liaison with external regulators (QIO, CMS/DOH/JC), vendors, corporate legal, quality, and population health (case management.
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Functional responsibilities for the incumbent include facilitating risk assessments to identify risk areas and risk mitigation measures, ensuring accurate and timely maintenance and review of validation and qualification documents for all equipment and facility activities; ensuring accurate and timely review of technology transfer documents; ensuring accurate and timely review of investigations and evaluation of change controls.
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Learns to recognize deviations from normal results and informs Study Director, Principal Investigator, Formulations Coordinator and/or management of any problems and/or deviations that may affect the integrity of the data.
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OR A Ph. D. or equivalent doctoral degree in a related field of study such as: Sociology, Business Management, Business Administration, Public Administration, Social Science, Environmental Science, Geosciences, Political Science, Law Enforcement, or other fields related to the petroleum industry.
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Experience in one or more of the following RIM systems i.e., Veeva Vault, PARAXEL/LIQUENT InSight, CSC Regulatory Tracker, ArisGlobal Register, OpenText, SharePoint, Documentum, FirstDoc / FirstPoint, NextDocs, CARA, Extedo eCTD Manager, Trackwise, or other regulatory information management systems or publishing tools.
$102,000 - $154,000 a yearFull-timeExpandUpdated Yesterday - UpvoteDownvoteShare Job
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Primary duties of the Trash Collector include: - Operating garbage trucks - Collecting and dumping trash receptacles - Following route assignments as directed Waste Management offers an excellent benefits package that includes medical, dental, vision, life, 401(k) savings and more.
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Someone who has experience as a project cost engineer or project accountant, minimum 3-5 years’ experience, experience with executive presentations etc. Experience as cost engineer or project accountant.
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We are seeking an experienced Senior Java Developer with a strong background in Finastra's Loan IQ platform to support project or production issues. Provide technical support for project and production issues, including troubleshooting and debugging.
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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.
$85,000 - $125,000 a yearFull-timeExpandUpdated Yesterday
project management engineer change controls jobs Company: Copeland in South Plainfield, NJ
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