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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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Support downstream process tech transfer, scale-up, clinical and commercial manufacturing as needed. Summary: This position will join a team of scientists/engineers focused on developing and optimizing manufacturing processes for gene therapy products for early- and late-phase clinical trials.
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Work as a Lead Mechanic on projects directing the activities of others.
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Our client, one of the largest Pharma companies in the U.S., is looking for a Investigator, MS&T (Manufacturing Science and Technology) which is located at Princeton NJ. Looking for MS&T Specialist to provide technical support and expertise in gene/cell therapy manufacturing processes.
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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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Vice President, Manufacturing & Plant Manager. 5-8 years of experience in a fully integrated manufacturing environment managing lean, continuous improvement and/or Kaizen programs and projects.
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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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Lead and drive the development of viral vector-based (e.g., AAV, lentivirus, retrovirus) manufacturing processes to improve efficiency, scalability, and product quality, with a focus on innovation and optimization.
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Central is home to a leading portfolio of more than 65 high-quality brands including Amdro, Aqueon, Cadet, Farnam, Ferry~Morse, Four Paws, Kaytee, K&H, Nylabone and Pennington, strong manufacturing and distribution capabilities and a passionate, entrepreneurial growth culture.
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We are looking for a Quality Control Biochemistry Analyst to join our team on-site in Hopewell, NJ. You will be responsible for QC biochemistry laboratory assay validation and transfer activities to support GMP manufacturing, testing and release of material, intermediates and finished products under FDA/EU regulations, applicable International Regulations, company processes and procedures.
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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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Minimum two years' experience within a chemical/food/perfumery manufacturing facilityMinimum of one through two years' experience in an manufacturing environment or handling of chemicalsKnowledge of G.M.P’s (Good Manufacturing Practices)Knowledge of H.A.C.C.P (Hazard Analysis Critical Control Pointsdsm-firmenich is fully dedicated to inclusion because when people feel engaged and empowered, their creativity and innovation drives unprecedented progress.
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Minimum 3 years relevant experience in GMP biologic/cell therapy manufacturing technical or process support. Experience with the start-up, validation, and licensure of new biopharmaceutical manufacturing facilities is a huge plus.
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These range from incubator companies focused on technology and cutting-edge diagnostics, to Fortune 500 entertainment, pharmaceutical, consumer products, publishing, consulting, manufacturing, and financial services firms.
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Ensure alignment of our R&D BCCM program vision, priorities, and plans with those of our partners in the BMS Enterprise Resiliency program, Manufacturing, Supply Chain, Facilities, Quality, IT (Cyber), and Third-Party Risk Mgmt.
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manufacturing job Title: representative Company: Gpac in Plainsboro, NJ
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