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Minimum of a Bachelors in a Science degree including but not limited to biology, chemistry, physics, chemical, mechanical or materials science engineering. CRM maintenance through the support of the Salesforce Coordinator and Marketing Manager.
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Creates, updates, and maintains written communication about requirements, deadlines, events, and other information related to doctoral students and faculty, including PhD and DrPH student handbooks, Canvas pages, student forms and other student-focused information and materials.
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Certified Hazardous Materials Manager. Serves as the Environmental and Safety Officer during disaster response emergencies and specifically directs the actions necessary to protect staff from exposure to hazardous materials.
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This position is responsible for assisting the Assistant Project Manager and Superintendent with shop drawings, submittals, scheduling of subcontractors and materials, meetings, as-built drawings, job cost, procurement, quality checks (inclusive of torque checks) and field operations.
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Coordinate, Develop format with Project Accountant for information transfer on labor, equipment, materials, subcontracts, and other direct costs for Estimate to Complete (ETC) projectionsCoordinate and update with Project Accountant on Monthly PSRs preparation Review of subcontractor invoices prior to PM approval and submit to Project Accountant for payment processing.
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Performing detailed research using Debtwire, PACER, S&P Capital IQ, Bloomberg, and other bankruptcy and restructuring related resources to identify prospects and prepare proposal materials. Assisting with the preparation of high-quality reports and presentations for clients.
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They need to improve information management for their labs (drug development); information like raw materials used, state of materials testing, etc. User Experience, Research & Development, Machine Design, Instructional Design.
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The Quality Systems Manager will be responsible for providing day-to-day support to ExM Operations on Quality Systems that enable business objectives to be achieved. The Quality Systems Manager will act as end-to-end Local Process Owner of one or more Quality Systems used within Global External Manufacturing.
$46.21 an hourFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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This role supports all three Nipro business units: Renal, Vascular and Med-Surg. The Supply Chain Planning Manager has the ultimate objective of mitigating risk to our business by developing and implementing strategies with Nipro factories and suppliers to ensure timely and continuous supply of quality products and materials.
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Pen/Pen Scripting, Python, UNIX/Linux, PL/SQL, Microservices, JIRA, Lean Kit, TDP, TOAD, SQL Developer, Rally, Selenium, Soap UI, Postman, XML, Quality Center, and Shell scripting. REQUIRES: Master’s or equivalent in Computer Science/Applications, Information Technology, Business Management/Administration or Electronics Engineering + 1 year experience as Software Quality Engineer, Software Quality Assurance Analyst, Test Engineer, Quality/Product Test Professional or related.
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Develop and thoroughly proofread copy for promotional materials including but not limited to event registration websites, emails, social media posts, flyers, banners, website pop-ups, and print pieces.
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Set-up, organize, and maintain clinical study documentation (e.g. Trial Master File documents, clinical study site documents, email correspondence, training materials, etc.) Prepare, ship and manage inventory of study related materials and supplies or coordinate the activities with the vendors, as applicable (e.g. CRFs, diary cards, ISF binders, etc.
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The Warehouse Manager will have general management responsibilities for our 3PL distribution warehouse and kitting and assembly facility located 5 minutes from our main operations facility. You will have management responsibility for material receipt, inventory control, order configuration, outbound processing, order/shipment quality, kitting project assembly, and other value-added services.
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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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The Quality Assurance Associate is responsible for reviewing laboratory processes, data, and reports of. Scientech Laboratories , in their search for a Quality Assurance Associate II. Assure all documentation (hard copy and digital) is complete, compliant, and of adequate quality to.
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materials job Title: quality manager in Piscataway, NJ
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