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The newly created Manufacturing Intelligence organization within Pfizer’s Global Technology & Engineering will help to drive Pfizer Global Supply toward ‘Industry 4.0’ capability through Big Data, Process Analytical Technology, Advanced Process Control, Artificial Intelligence and Robotics.
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CGMP manufacturing experience, preferably cell/gene therapy, with experience in tech transfer, process validation, project management, and change management. This individual will oversee process engineering, manufacturing support, technology transfer, validation, and cell therapy automation and provide technical and continuous improvement support to ensure robust production, testing, and the timely release of cost-effective, compliant, and high-quality cell therapy products.
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This role will partner with multiple Legends CARVYKTI Collaboration partner teams, such as Demand Planning, Supply Planning, Manufacturing, Vein to Vein, Finance and Commercial Operations, as well as internal stakeholders across the Global Manufacturing & Supply network.
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You're considered fully vaccinated two weeks after you receive the second dose of a two-dose vaccine series (e.g., Pfizer or Moderna) or two weeks after a single-dose vaccine (e.g., Johnson & Johnson/Janssen.
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Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a CAR-T Manufacturing Batch Advocate, Senior Analyst! Minimum of a bachelor's or equivalent University Degree required; focused degree in Immunology, Molecular Biology, Bio-Pharmaceutical Manufacturing, or equivalent field preferred.
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Supervisor, Manufacturing Operators. 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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Minimum 3+ years of industrial biologics CMC development or manufacturing experience, Cell therapy manufacture experience is highly desirable. Manage the CMO tech transfer and clinical/commercial manufacture: trouble shooting problems, conducting investigations, track timeline and KPIs, overseeing capacity expansion, monitoring budget, driving cost reduction and quality improvement and serve as Person in Plant.
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This position will be responsible for metrology support for cGMP Clinical and Commercial Cell Therapy Manufacturing. This individual will partner with various Technical Operation functions in support of personalized cell therapy production through safe and compliant manufacturing operations according to cGMP requirements.
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Partner with Manufacturing, Product Support, Microbiology, Regulatory Affairs, Quality Control Labs, Engineering and Compliance. Utilize multifaceted industry and process excellence standards on an expert level in daily quality operations, including good manufacturing practices (GMP), and international organization for standardization (ISO.
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Position Description: The Automation Engineer is primarily responsible for leading projects, the development and/or configuration of PLC/HMI codes, S88 batch recipe, historian data, historian reports, data analytics for reliable operation of manufacturing processes, and the existing automation systems, support for Building Management System (BMS), Utility and manufacturing process automation support for the Lilly New Jersey Facilities, as applicable.
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The newly created Manufacturing Intelligence organization within Client's Global Technology & Engineering will help to drive Client Global Supply toward 'Industry 4.0' capability through Big Data, Process Analytical Technology, Advanced Process Control, Artificial Intelligence and Robotics.
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Alfasigma USA is headquartered in Bedminster, NJ. with a manufacturing plant in Shreveport, LA., a remote mail order pharmacy call center and an established national salesforce. Alfasigma is a leading Italian pharmaceutical company focused on prescription drugs, over-the counter (OTC) and nutraceutical products and has a presence in 90 countries.
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Good knowledge of pharmaceutical manufacturing and related unit operations is also a plus. The successful candidate will be a member of the SMO team and will have the responsibility to develop and implement Process Analytical Technologies, and support robotics, cobotics and lab automation initiatives for SMO manufacturing and quality operations.
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We are seeking an innovative and highly motivated Senior Director, IT GMP Systems who will play a critical role in the launch and ramp-up of a state-of-the-art multi-product cell therapy manufacturing facility that will be utilized to manufacture autologous and allogeneic cell therapy products.
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Reporting to the Global Quality Engineering Director, the Supplier Quality Specialist will achieve ALAM goals in the areas of manufacturing quality, technology advancement, productivity, off-spec elimination, non-conformance elimination, customer satisfaction, and cost reduction.
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pfizer manufacturing jobs in Far Hills, NJ
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