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The Manufacturing Supervisor may be assigned to work directly with Upstream, Downstream or Buffer Preparation Unit Operations. Develop, write, and review Standard Operating Procedures, Buffer Formulation Records and Batch Production Records (BPRs.
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Perform routine production activities such as upstream and downstream processing, purification, and formulation. Perform routine production activities such as upstream and downstream processing, purification, and formulation.
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Problem formulation and solutioning; Hypothesis framing; Business strategies; Business management practices across multiple domains; Customer segments and needs; Domain-specific knowledge; "Go to Market" strategies; Industry, environmental, and economic factors and competitors; Product discovery process, product vision, product strategy and challenges; Rapid prototyping and Lean experimentation methodologies; Concepts of "First Principle.
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The formulation scientist will work closely with downstream and analytical scientists to analyze biochemical and biophysical properties for biopharmaceutical products. Support and closely work with research, cell-line development, upstream, downstream, and analytical scientist.
$90,000 - $120,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Qualifications: Bachelor's degree in Biotechnology, Biochemistry, Molecular Biology, or related field. Required) Familiarity with cGMP regulations and industry standards for biopharmaceutical manufacturing.
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Communicate and collaborate within Analytical Development and cross-functional areas (Upstream, Downstream and Formulation Developments) The successful candidate will learn size exclusion chromatography theory, operation of Agilent and Waters LC instruments, wet chemistry lab skills, data analysis with Empower software, chromatography data interpretation, and documentation of experimental results using an electronic lab notebook.
$20 - $22 an hourInternExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Required Skills: Buffer formulation, lab equipment operation such as Akta Avant, peristaltic pumps, pressure sensors, pH probes, pipet operation, UV spectrophotometry Experimental design with proteins Theory of Protein ion exchange and affinity chromatography or affinity precipitation Desired Skills: Fundamental and practical understanding of downstream unit operations Arduino programming and building prototypes Experience with GMP equipment design and use of data management systems.
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Technical experience with downstream unit operations including clarification, TFF, chromatography, sterile filtration and formulation. The Principal Scientist will serve as the downstream processing expert working closely with CDMOs to generate lentivirus and adenovirus products.
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About the team: The Contingent Workforce Management team is responsible for ByteDance's Policy formulation and system construction related to contingent workforce worldwide, providing comprehensive contingent workforce solutions to help business compliance and efficient use of contingent workforce resources.
$165,120 - $399,600 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Execute and monitor critical processes for mAb manufacture such as media and buffer preparation, upstream expression, downstream purification, formulation, fill / finish, and secondary packaging.
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Subject Matter Expert in cGMP downstream manufacturing; especially with Chromatography, Column Packing, Tangential Flow Filtration (TFF), Ultrafiltration/Diafiltration (UF/DF), Nanofiltration, Formulation, Bulk Drug Substance Aliquoting.
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Downstream unit operations include harvest, clarification, chromatography, centrifugation, TFF (UF/DF), filtration, formulation, and fill-finish. The position will be responsible for performing upstream and downstream bioprocessing procedures to support the commercial manufacturing of native antigens, recombinant proteins, antibodies, and blockers.
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As a Senior Process Engineer , you will provide guidance to develop and implement process concepts and designs on projects related to Gene and Cell Therapy, Formulation and Filling and facility utilities.
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6+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, and bulk formulation. REGENXBIO is currently searching for a Gene Therapy Manufacturing Supervisor (Downstream) to help us build our team.
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0-2+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, bulk formulation and/or fill finish.
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downstream formulation jobs
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