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The ideal candidate for this position should have work experience in cell therapy process development, manufacturing science, analytical development, and familiarity with GMP/FDA/ICH. Catalent Pharma Solutions in Princeton, NJ is hiring a Senior Scientist, Cell Therapy Process Development who is responsible in contributing to the development of early and late stage clinical cell therapy manufacturing processes.
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The ideal candidate for this position should have work experience in cell therapy process development, manufacturing science, analytical development, and familiarity with GMP/FDA/ICH guidelines.
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Actively looking for a Senior Scientist, Cell Therapy Process Development contributing to the development of early and late stage clinical cell therapy manufacturing processes. Experience with common equipment used in cell therapy manufacturing such as Sepax, Lovo, G-Rex, Xuri Bioreactors, CliniMACs Plus, CliniMACS Prodigy, MaxCyte GT.
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Initiate Change Controls and complete necessary documentation;Collaborate with cross-functional teams, including Quality Assurance, Manufacturing, and Research & Development;Support developing and implementing the site Microbial Control Strategy from incoming raw materials through final product release.
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Job Description :Actively looking for a Senior Scientist, Cell Therapy Process Development contributing to the development of early and late stage clinical cell therapy manufacturing processes.
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Review and approve contractor’s manufacturing, packaging, and analytical records for data integrity and GMP compliance and consistency with company policies and procedures necessary for Quality disposition of clinical intermediates, API and finished drug products at Novo Nordisk.
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Our Team Georgia-Pacific's Naheola Mill located in Pennington, Alabama, is a manufacturing site for the company's well-known consumer products business. Actively plan prioritize work requests from area gatekeeper and Manufacturing Engineers.
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Experience with at least one of the following preferred: moving, warehouse, manufacturing, inventory management, stocking, forklift, shipping and receiving, helper or general labor. As a Warehouse Associate, you will be expected to lift and carry items weighing up to 50lbs regularly.
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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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Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
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Minimum 3 years relevant experience in GMP biologic/cell therapy manufacturing technical or process support. Must Have Gene/Cell Therapy Manufacturing experience. Experience with the start-up, validation, and licensure of new biopharmaceutical manufacturing facilities is a huge plus.
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Description/Comment: - ONSITE POSITION - DURATION - MINIMUM MONTHS AND MAY BE TEMP TO HIRE FOR RIGHT CANDIDATE - SHIFT - MON-FRI AM TO PM - MUST HAVE - GENE/CELL THERAPY MANUFACTURING EXP. The MS&T Specialist provides technical support to Princeton, NJ Facility.
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Provides on-the-floor and on-site technical support to manufacturing when necessary. Analyze and summarize manufacturing data to support impact assessments and investigations. Technical support includes troubleshooting process and equipment related issues that occur during the Manufacturing process.
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The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas About UsIPS, a Berkshire Hathaway Company, is a global leader in developing innovative business solutions for the biotechnology and pharmaceutical industries.
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3-6 years of experience in Clinical Research Associate (CRA) tasks, including remote monitoring, SOP creation, site selection setup, and protocol development. Position Summary: The Senior Clinical Research Associate (Sr. CRA) will be responsible for overseeing and executing various clinical research activities, including remote monitoring, protocol development, site selection and setup, and SOP creation.
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manufacturing job Title: associate research market in Princeton, NJ
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