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The successful candidate will work in the laboratory as well as with Contract Development/Manufacturing Organizations (CDMOs) to ensure all aspects of the drug substance process development and manufacturing are completed according to Quality by Design principles and cGMP requirements.
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Collaborate with process development scientist to get trained and transfer new processes into cGMP manufacturing. Master's degree in chemistry, biotechnology, biology, engineering or related pharmaceutical science and 2+ years relevant cell processing experience (1+ years direct experience working with cell therapy autologous or allogenic programs) in Manufacturing.
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De)manufacturing including alternatives for feedstocks and degradation of the products, synthetic biology tools for sustainability, life cycle analysis, catalysis, recycling/upcycling , plastics/microplastics, carbon capture, renewable and sustainable consumer products, and process intensification.
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Lead an Attribute Sciences team to support synthetic small molecule, synthetic peptide, and/or SiRNA drug substance and drug product process development, manufacturing, release & stability testing and characterization.
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As a Process Engineer your role is to focus on the planning, design, operation, control, optimization, and intensification of chemical, physical/mechanical, and biological processes for complex water/wastewater treatment facilities and pumping stations.
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Proven laboratory expertise in radioactive product development or manufacturing, radiochemistry, including radiochemical separations and chemical synthesis. QSA Global, Inc. specializes in supplying state of the art gamma radiography and portable X-ray systems used in non-destructive testing (NDT) as well as high-performance radiation sources used in oil well logging (OWL), industrial processes, and nuclear medicine.
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Work closely with colleagues in Process development to design and implement new technologies for aseptic filling of cell therapy drug products in novel device platforms; this includes working closely with Contract Development and Manufacturing Organizations (CDMOs) and engineering firms to design processes and equipment needed to perform aseptic filling operations in a GMP environment.
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Prospect biotech and pharmaceutical companies seeking CGT process development and manufacturing partnerships that fit the ElevateBio BaseCamp strategic goals and objectives. The ElevateBio ecosystem combines multiple R&D technology platforms – including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform – with BaseCamp, its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.
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Bachelor’s degree in chemical engineering, materials engineering, polymer science & engineering, or related education. Work closely with Senior R&D Engineers to operate CVD chambers, producing both conductive and waterproof fabrics, and eventually learning to perform depositions independently.
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Experience in engaging regulatory professionals for navigating the product development process through FDA regulatory submission, scaling manufacturing, and post market surveillance. We’re looking forward to bringing on our next Mechanical Design Engineer to work alongside our CTO. You’ll have ownership over our auto-injector’s assembly process from start to finish.
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We have developed a drug-discovery platform that integrates computational chemistry, structural biology, chemical biology, target-informed screening, and mechanism-driven pharmacology to develop small-molecule therapeutics that specifically modulate ferroptosis.
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Execute new technology development initiatives to enhance manufacturing capabilities (such as media development, bioreactor fed-batch and perfusion process development, optimization and scale-up.
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MERGE has enduring client partnerships with American Express, T-Mobile, LG, Kate Spade NY, Coach, The Northface, Meta, Subway, BlueCross BlueShield, Abbott, Supernus, Seqirus, GE Healthcare, CVS/Aetna, Brigham Health, Indiana University Health, and Eaton Vance to name a few.
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Analytical Skill, Analytical Skill, Analytical Thinking, Chemical Biology, Chemistry, Clinical Trials, Collaboration, Communication Skills, Curiosity, Data, Data Analysis, Design Of Experiments, Detail-Oriented, Drug Development, Drug Discovery, Ethics, Gene Therapy, Immunology, Inventory Management, Laboratory, Lifesciences, Machine Learning (Ml), Management, Medical Research, Molecular Biology {+ 10 more.
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PhD in Pharmaceutics, Biotechnology, Biomedical Engineering, Chemical Engineering, Biology or related field with a strong background in gene therapy-based drug product development and 3+ years industry experience.
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