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Use of Valor NPI, Design for Manufacturing rule sets, other Design Rule Checking software. Technical PCB design skills using the Siemens design toolset including, but not limited to the Xpedition Layout tool suite with working knowledge of schematic capture, placement, routing, use of the auto-router, constraint manager, and library tools, and use of BluePrint to create complex PCB and CCA drawings, Altium is not used, but transfers over well to the Siemens toolset.
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The Manufacturing Engineer will apply engineering principles to design and improve casting operations and will report to the Engineering Manager. The Casting Manufacturing Engineer will help to optimize and enhance the casting process and will collaborate closely with cross-functional teams to ensure the production of high-quality automotive components, while continuously striving for process improvement and cost-effectiveness.
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As the product design expert for activities downstream of product development, work with NPI/Manufacturing in the successful transition of the product into both LRIP and FRP. Product Sustainment in Production.
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Our diverse list of clients allows us the unique ability to work across industry lines in the oil and gas upstream and midstream as well as chemical and petrochemical downstream, industrial manufacturing, power generation, renewable energy, mission-critical, heavy-commercial, and energy storage sectors.
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Demonstrate core Manufacturing Engineering functions:Coordinate the design and procurement of manufacturing fixtures, tooling, gauges, and test equipment integral to the manufacturing process.
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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. Previous work history with PCB manufacturing or CCA manufacturing principles that affect circuitry and component layout along with RF specific layout techniques.
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This person will join a fast-paced, collaborative, and multidisciplinary team to support bioreactor process development (perfusion and intensified fed-batch) at the bench and pilot scale for the advancement of low-cost biotherapeutics manufacturing.
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Typically requires a Bachelor’s in Science, Technology, Engineering, or Mathematics (STEM) and a minimum of 2 years of prior relevant experience, to include at least two (2) of the following: Previous work history with PCB manufacturing or CCA manufacturing principles that affect circuitry and component layout along with RF specific layout techniques Experience with the electrical design process including RF layout History with laying out Rigid, Flex, or Rigid-Flex boards.
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Awareness of Valor NPI, Design for Manufacturing rule sets, other Design Rule Checking software. The Product Design and Packaging (PDP) Team at Raytheon is seeking a Principal Electrical Engineer to join our team as an Electrical Computer Aided Designer Engineer (ECAD.
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In this vital role you will lead a Downstream Process engineering team at our Rhode Island Site. The Senior Manager will lead a team focused on bioprocess purification processes, drug substance manufacturing support and technology transfer of new products into the facilities.
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Design, optimize, and scale-up downstream processes for the purification of viral vectors, with a focus on AAV and lentiviral vectors. Collaborate with cross-functional teams, including Upstream Process Development, Analytical Development, and Manufacturing, to ensure seamless integration of processes.
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In this vital role you will be responsible for planning, design, construction, operations and maintenance technical support of Amgen manufacturing infrastructure, world-wide. Strong understanding of GMP equipment design and biologics manufacturing requirements.
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Understand and incorporate downstream manufacturing operation requirements into AM design models (e.g. machining stock, dimensional impact from heat treat and HIP operations). They have experience with additive manufacturing design processes, and the impact of downstream operations to overall product design.
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As a scientist in the Purification Development group, you will identify and develop new purification technologies, work to design optimized downstream drug substance processes for new biologic candidates, employ strategic thinking to overcome technical hurdles and oversee process technical transfer to GMP manufacturing facilities, as they make their way from discovery to the clinic and eventually commercialization.
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Participate in design of experiments for chromatography, harvest clarification, virus removal filtration, UF/DF, and any other required downstream process steps. The Senior Associate Scientist may also be responsible for supporting Technical Transfer, Manufacturing investigations, and Regulatory filings related to downstream process stages.
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