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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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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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Participate in post-project analysis to identify lessons learned and opportunities for continuous improvement in the product development process. The Program Manager will work with a global team of project managers, engineers, and supply chain, operations, and manufacturing personnel to deliver well-planned, well-executed development projects on time, within budget, and to appropriate quality and performance standards.
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Additionally, you will contribute to and be responsible for all engineering aspects of multi-discipline projects in various markets and business including: Water (Water/Wastewater Treatment, Linear Water, Water Resources) Energy and Resources (Chemicals, Oil & Gas, Future and Renewable Energy, Industrial Manufacturing), Environmental (Solid Waste, Landfill, CAR), with potential future work in Transportation (Highways, Roads, Bridges, Rail, Transit.
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Assist in the release and shipment of finished product from the manufacturing site to the 3PL warehouse facility. Communicate Solaris requirements (product forecasts) consistently with manufacturing sites and vendors to ensure that there is sufficient inventory of product at our warehouse.
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O Minimum 3-5 years of industry experience (IT, Manufacturing, Production, BFS, etc.) Continuous Integration Tools (Jenkins, Cruise, TeamCity, Hudson, etc) o Minimum 10 to 12 years' experience in Agile and Lean based process improvements in a large organization acting in a leadership role /Managing Consultant /Client Program Manager.
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The position interfaces with experts in Process Development, Analytical Development, Manufacturing Sciences and Technology, Operations, Quality and Regulatory Sciences. 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.
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If you’re looking to build a career in manufacturing with a team and facility that values safety and quality, we might be the team for you. The Clark manufacturing facilities have 9 work centers with processing capabilities in Liquid Flavor Compounding, Dry Blending, Extractions, Distillations, Spray Dry, Emulsions, Essential Oils, Oleo Resins, Juice Blending.
$27 an hourFull-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Our commitment to continuous growth since 2018 has earned us the #3 spot on the SMU Dallas 100 List, and it is thanks to our amazing team that Advantis Medical has also been awarded the USA Top Workplace in 2023, Regional Top Workplace in 2022, and named the Dallas Morning News Top 100 Places to Work in 2021.
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The Environmental Permitting Project Manager can report to the New Providence, NJ or Mount Laurel, NJ offices, the New York, New York office, or the Philadelphia, PA office (with an option to work remotely) and will support development, implementation, maintenance, and improvement of key permitting programs to support quality and strategic growth plans.
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Job Description: We're looking for a Senior Application Analyst with experience in mainframe systems.
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Marmon Industrial Water is currently seeking an Instrumentation & Controls Engineer to join our New Equipment group. Our technologies included raw water pretreatment, degasification, hot lime softening, boiler make-up, condensate polishing, wastewater treatment, cooling, and oil/water separation for markets such as petrochemical/chemical, power generation and heavy industrial plants.
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Works on continuous improvement programs for improving the steps and timelines from evaluating desired geo markets to product launch. Supply Chain, Regulatory, or Pharmaceutical manufacturing experience working with third party suppliers.
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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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Hard SkillsGlobal clinical trial managementVendor and CRO managementProcess improvement initiativesDeveloping study-specific documentationRisk assessment and mitigationCTMS & TMF System - Veeva VaultBudget and timeline managementSoft SkillsLeadershipSupervisionMentoringPerformance managementCommunication.
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continuous improvement lean manufacturing jobs Title: quality engineer Company: Trinus Corporation in Warren, NJ
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