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The Advanced Manufacturing Engineer - Forge will lead and support forging process development for medical device products across the company. Bachelor's degree in one of the following disciplines is required: Forge Engineering, Mechanical Engineering, Materials Science Engineering, Manufacturing Engineering, Industrial Engineering or Chemical Engineering.
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Direct the planning and implementation of process development, scale-up, technology transfer, and validation efforts in drug substance manufacturing, ensuring strategic alignment and operational excellence.
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FirstPRO is now accepting resumes for an SMT Manufacturing Engineer to provide technical engineering support to manufacturing printed circuit boards utilizing surface mount technology (SM'J') and through-hole technology (TH.
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Experience with current technologies in iPSC process development and manufacturing, particularly scalable stem cell culture systems such as bioreactors. You will define and execute process development and tech transfer activities to enable iPSC expansion and differentiation in GMP manufacturing throughout the product lifecycle.
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Knowledge of advanced manufacturing methods: Additive manufacturing, EDM, rapid prototyping, casting and molding, laser cutting, laser welding, injection molding, soldering, etc. Knowledge of advanced manufacturing methods: Additive manufacturing, EDM, rapid prototyping, casting and molding, laser cutting, laser welding, injection molding, soldering, etc.
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Job Summary: The Manufacturing Engineering Manager is responsible for leading and overseeing the engineering and production processes with a focus on deep hole drilling, CNC programming, setup supervision, and maintenance.
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Process Engineer Position Summary:Catalent Pharma Solutions is Chelsea, MA is hiring a Process Engineer who is responsible for assisting senior engineering staff in the design and implementation of manufacturing processes, instrumentation and equipment for clinical and commercial manufacturing.
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Familiarity with computerized pharmaceutical GMP systems such as LIMS, CDS, BMS, JDE, SAP, Analytical Instrumentation, Manufacturing and Packaging systems, Quality Management Systems, and their associated vendors.
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Act as the key contact to SQF practitioner, OSHA and for all plant manufacturing practices & maintenance. Contact: John@SourceRecruitmentSolutions.com Our client, a premier Food Manufacturing Company with products sold nation wide is seeking an experienced Quality Assurance Manager.
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Its patent-pending and proprietary pluripotent stem cell differentiation technology platform TFomeTM was developed in Professor George Church’s lab, a pioneer in synthetic biology, and allows for the development of unique cell therapies with significantly streamlined manufacturing, improved cell quality, efficiency and speed.
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Hands-on knowledge of cGMP and CMC regulatory requirements for cell or gene therapy manufacturing. As we strive to halt degenerative diseases, we seek talented CMC leadership to lead tech transfer to our late-phase and commercial CDMO, manage DP production for our Phase III trials, prepare the CMC strategy for BLA submission, and build a manufacturing organization for commercialization.
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Poly6 is enabling production of complex turbine engine designs by combining additive manufacturing with advanced materials. · 1+ years’ experience in additive manufacturing for industrial manufacturing.
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Prior experience must include: Perform purification process, including experimental planning, sample handling, method creation; Conduct tech transfer for manufacturing sites; Analyze experimental data using JMP; Write technical documents; Monitor GMP manufacturing and related in-process controls; Implement new technology associated with continuous processing; Develop and transfer methods (purification process & analytical.
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Experience in technology transfer to Contract Development and Manufacturing Organizations (CDMOs) for both non-Good Manufacturing Practices (non-GMP) and Good Manufacturing Practices (GMP) manufacturing, encompassing cell line development, process development, and scale-up.
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This role is suited for an R&D engineer with experience in developing, building, and testing complex electro-mechanical medical devices, design transfer, and process validation with broad knowledge of electrical, mechatronics, firmware, software, and systems engineering, including design verification testing, and transfer to manufacturing within a regulated medical device development environment.
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manufacturing job in Watertown, MA
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