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Work tasks may involve the development, management and/or oversight collection of data, alternative analysis evaluation for engineering reports, horizontal and vertical alignments, cross section and superelevation design, roadside barrier design, ADA curb ramp design, roadway modeling, roadway plans, erosion and sediment control plans, stormwater management plans, right-of-way plans, utility relocation plans, permit application drawings, and traffic control plans.
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Keywords: Surveyor, land surveying, field operations, data collection, ALTA surveys, topographical surveys, construction surveys, Leica total stations, GPS, 3D laser scanners, outdoor work, overtime, computer literacy, communication skills, growth, development.
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Collectively, the team is accountable for CMC activities encompassing cell line development, cell culture/ microbial fermentation, purification development, and drug product/ device development.
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As Sr. Manager CMC Regulatory Affairs you will also be responsible for identifying and evaluating CMC issues associated with development products, including product and process development, analytical methods, formulation development, manufacturing, and labeling.
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The IT Sr. Solutions Engineer will lead the design and configurations of CertainTeed / Saint-Gobain Information Technology and Salesforce.com development initiatives, providing industry best practices around force.com technologies and beyond.
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As Scientific Director, Upstream Process Development within Biopharm Drug Substance Development, you will provide strategic leadership of scientific and organizational objectives related to portfolio projects and technology initiatives.
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Conduct experiments and perform analytical testing using standard laboratory techniques including: Standard microbiology Enzyme assays Product efficacy evaluation P Research Associate, Research, Associate, Microsoft, Product Development, Microbiology, Manufacturing, Technology.
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Trains junior Software Development and Operations Engineers. Responsible for planning, designing, building, monitoring, and supporting new and existing software and web applications in a team of Software Development Engineers in a Global DevOps environment.
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We are seeking for our Philadelphia-based R&D laboratory a creative, motivated Research Associate/Scientist with expertise in cell biology laboratory techniques to contribute to the development of our novel, cell-penetrating peptide-based platform for biologics delivery.
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The Scientist, Upstream Tech Transfer (PD/Tech Transfer) will report to the Associate Director of Tech Transfer and will have responsibilities supporting the upstream process development. Work closely with process development scientist and/or client in process knowledge transfer to scale-up process for pilot scale.
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Employs software development techniques to implement tests that support automation on CI/CD. Full stack development experience on AWS Cloud native apps. Provides level system analysis, design, development, and implementation of applications and databases.
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Serving patients in over 50+ communities, OIA is an imaging center management & development operation that is committed to delivering an affordable diagnostic imaging option without compromising customer convenience, care, technology or results.
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10 years of experience with various Software Development Life Cycle methods such as Agile, SCRUM, Waterfall, etc. The Sr. Data Engineer is responsible for playing the role of ETL/Snowflake Technical Lead. The chosen candidate will lead the team of data engineers in understanding and supporting the businesses through the design, development, and execution of Extract, Transform, and Load (ELT/ETL), data integration, and data analytics processes for a migration of an Azure Data Lake to a new Snowflake database.
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Supplier Management - Perform Supplier Management: Supplier Qualification, documentation and communication of strategic and key supplier s data, regular supplier and strategic evaluations and supplier development to obtain and develop the best suppliers and to ensure an optimized supply chain.
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The Clinical Trial Supply (CTS) Asset/Program Lead (Associate Director) is an experienced clinical supply chain professional accountable for the development and execution of the clinical supply operational strategy for an asset or program (a group of related, typically larger and/or more complex, clinical studies) throughout the multi-year lifecycle.
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development job Title: software eng Company: Autodesk in Malvern, PA
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