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Collaborate closely with development, manufacturing, quality, and regulatory teams to align tech transfer processes with project timelines and objectives. Cross-functional tech transfer experience Bachelor’s degree in STEM/Life Sciences-related discipline Project management qualification preferred Proficiency with related software tools such as: MS Project, Office Timeline Pro, Smartsheet, MS PPT, MS Excel, SharePoint, etc.
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Working conditions require the ability to sit, stand, walk, bend, climb stairs, and work at a computer station and on the manufacturing shop floor. Monitor, review, and improve manufacturing and quality-related activities and drive corrective and preventative actions.
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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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Kelly Science is seeking a Nuclear Pharmacist for a growing manufacturing facility located in Somerset, NJ. Provide on-the-floor QA oversight of manufacturing, QC, and other cGMP activities.
$116,000 a yearFull-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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Experience in power generation, renewable energy, pharma, petrochemical, heavy industrial, or manufacturing is highly regarded. Manage and execute projects in industries such as power generation, renewable energy, pharmaceuticals, petrochemicals, and manufacturing.
$155,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Job Type: Senior Tax Analyst Location: Somerset, NJ Pay: $40/hr+ An international manufacturing company is looking for a Senior Tax Analyst to assist their team in preparation of the Indirect Tax compliance process.
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The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconductor manufacturing and metrology, to a broad range of scientific R&D and QC measurements.
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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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Work with our software team on integration solutions for the manufacturing process and data management, including eBR, MES, QMS, and LIMS. We are seeking an innovative and highly motivated Senior Process Engineer on our MSAT team who will contribute significantly to the development of our advanced cell therapy manufacturing platform.
$210,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Prior experience working in a pharmaceutical, biotech, or food manufacturing environment is preferred, regulated by GMP standards and requirements. On site we have our state-of-the-art laboratory, clinical, and commercial manufacturing plant for oral dose forms in addition to being the Catalent Center of Excellence for handling Highly Potent Active Pharmaceutical Ingredients.
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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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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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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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To support further expansion, the Upstream Manufacturing Scientist will be responsible for executing mammalian cell culture processes and producing proteins for a wide range of mammalian based biosimilars.
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3 or more years of GMP Operational or Pharmaceutical Manufacturing scheduling experience required. Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide.
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pfizer manufacturing jobs in Raritan, NJ
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