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Industry giant seeks an experienced Process Development Scientist to develop protein purification processes to be scaled up and transferred into cGMP manufacturing including evaluation of transferred processes, transfer of processes to manufacturing, harvest clarification, normal flow filtration, purification, tangential flow filtration, and product final formulation.
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Reports to: Staff Scientist, Downstream Development for Protein Development and Manufacturing Location: San Carlos, CA Compensation: The compensation package will be competitive and includes comprehensive benefits and an equity component.
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Responsible for Printed Circuit Board (PCB) designs from conception to manufacturing. Utilizing software such as Siemens: Xpedition Enterprise and DownStream Technologies: BluePrint-PCB. Awareness of Valor NPI, Design for Manufacturing rule sets, other Design Rule Checking software.
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Minimum of 3 years’ working with clients/projects in one of the following industries - Energy (Upstream or Downstream or Oil/Field Services), Chemicals, Retail, Consumer Products, etc. Minimum of 5 years’ experience with S/4 HANA and/or SAP Ecosystem Applications (ie: SuccessFactors, Ariba, Analytics, Manufacturing Cloud, etc.
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The Company is vertically integrated from mined raw materials, direct reduced iron, and ferrous scrap to primary steelmaking and downstream finishing, stamping, tooling, and tubing. Working rotating shift work in a 24/7 manufacturing environment.
$35.47 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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REGENXBIO is currently searching for a Gene Therapy Manufacturing Supervisor (Downstream) to help us build our team! Opportunity to work in an "ALL" stream environment that allows for cross-functional development between the differing manufacturing areas, i.e. media/buffer prep, upstream (US), downstream (DS.
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A fast-growing vaccine company is looking to a hire an energetic and talented individual to manage and operate the downstream pilot-scale operations in our San Carlos pilot plant facility within the protein process development and manufacturing group.
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Successful candidates will have a degree in Chemical Engineering, Biological Science or related discipline and preferably have experience with some of the techniques utilized for either upstream (e.g. mammalian cell culture in controlled bioreactor systems) or downstream (e.g. liquid chromatography methods) manufacturing processes.
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B.A./B.S degree in Chemical Engineering, Biology, or similar relevant field with at least 6 years of direct GMP manufacturing experience in a biotechnology manufacturing facility or Pilot Plant OR a High School Diploma with 10 years of experience in protein purification in Biotech/Pharmaceutical industry.
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The Manufacturing Supervisor may be assigned to work directly with Upstream, Downstream or Buffer Preparation Unit Operations. Masters degree in Biology, Microbiology, Chemistry, Biochemistry, Engineering, or related field and 3+ years of experience in a manufacturing environment; OR.
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Manufacturing cGMP production activities include solution preparation, master/working cell bank production, upstream cell culture, downstream protein purification, mRNA and molecular therapeutics production, and small-scale fill/finish.
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You’ll gain a deep understanding of capital projects management, facility design, storage and order fulfillment systems design for distribution networks, material flow automation, intersection of WCS/WES and WMS. The scope includes parts arriving at Tesla's network of warehouses then downstream manufacturing facilities.
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The successful candidate will have a strong technical understanding of development and CMC activities for antibodies including cell line development, manufacturing as well as upstream and downstream process development.
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BASIC REQUIREMENTS Downstream Process development experience, Chromatography, TFF-UD/DF, micro filtration, nano filtration, and filtrationDownstream processes at the small to an intermediate scale of cGMP biologics production.
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Coordinate multiple aspects of projects/processes within area (GMP/ECTL) with guidance, and execute processes (e.g., tech transfer & scale-up runs, HPLC/biologic assays, manufacturing of cellular therapeutics) utilizing appropriate techniques, equipment, and methods.
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