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The Manufacturing Associate III is responsible for advising and supporting the overall GMP manufacturing process, through the application of broad knowledge of theories and principles utilized to perform operational, as well as routine tasks in the production of cell therapy and/or human cells cultivation.
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The Talent Acquisition Manager works within the HR department both at the pharmaceutical manufacturing facility at the East Windsor, NJ location and corporate headquarters in Princeton Junction, NJ. This position works onsite four days per week.
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We are seeking a skilled and motivated DeltaV MES (Syncade) Engineer to join our pharmaceutical manufacturing team. The DeltaV MES (Syncade) Engineer will be responsible for the implementation, maintenance, and optimization of our DeltaV and Syncade systems, ensuring seamless integration with our manufacturing processes.
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Cross-functional interaction, coordination, and planning/scheduling with Perfumers, Fragrance Development Managers, account teams, sample labs and QC/Manufacturing Knowledge of basic perfumery raw materials and their overall stability in alcohol solutions and line extensions with the ability to identify high risk materials.
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Overview: The Microcircuit Emulation Center at SRI International (formerly Sarnoff Corporation) is looking for a Wafer Fab Integration Engineer to support the manufacturing of microcircuits (integrated circuits) on-site at our Princeton, NJ office.
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These digital solutions span across the BMS value chain from clinical trials to manufacturing, to commercialization and market access. In this role, you will lead the legal support, including directly advising, educating BMS colleagues, staying current on evolving global regulatory, legal and policy environment for BMS’ work with digital solutions, including regulated patient and physician-facing digital health solutions (e.g., digital medicine and digital therapeutics) such as mobile applications, diagnostic algorithms, digital biomarkers, use of artificial intelligence and clinical decision support solutions.
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Job DescriptionAt IPS, you’ll apply your knowledge, skills, and passion to make a difference in the lives of people, solving complex challenges related to pharmaceutical, biotech, and animal health research and manufacturing facilities.
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Certifications in Reliability (CMRP), Lean / Six Sigma Green Belt and/or Black Belt or equivalent experience leading in a Lean/TPM manufacturing environment. Minimum of 7+ years of progressive experience working in Lean Manufacturing, Technical, Maintenance, Reliability and Operations Management within a manufacturing environment.
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The GRS-CMC Associate Director, Biologics will assess Manufacturing Change Controls for global impact and guide technical teams on practical aspects of global change management. The team also perform regulatory assessments for manufacturing changes, provides guidance on regulatory expectations for medical devices, oversees BSE program and provides compliance documents to support Health Authority submissions.
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All three major manufacturing departments utilize filtration technologies. Responsible for providing support to their respective process team, per Manufacturing Standard for Operational Excellence (MSOE) 602.
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In this role, the CMC Regulatory Manager will serve as the primary interface between Global Regulatory Sciences (GRS) & Global Product Supply (GPS) The GRS-CMC senior manager will assess Manufacturing Change Controls for global impact & guide technical teams on practical aspects of global change management.
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Our four integrated businesses - Roofing, Insulation, Doors, and Composites - provide durable, sustainable, energy-efficient solutions that leverage our unique material science, manufacturing, and market knowledge to help our customers win and grow.
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The Associate Director Manufacturing (US) provides operational leadership to drive and expand the global network of decentralized point-of-care manufacturing units for CAR-T cell therapy.
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GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
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5 or greater years of experience designing, commissioning and starting up chemical plants, semi-conductor manufacturing facilities and performing hands-on optimization of specialty chemicals/gases or semi-conductor production units.
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manufacturing job in Hopewell, NJ
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