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Possess continuous improvement experience with emphasis in the laboratory information management and deployment of LEAN/Six Sigma, analytical methods and manufacturing process development for polymeric materials.
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Job DescriptionGeneral Summary:The Sr. Manager, Manufacturing Technical Operations (MTO) is responsible for managing compliance related Quality records including, but not limited to, Deviations, CAPA’s, Change Controls, Risk Assessments and Analytical and Quality Control Investigations supporting Biopharma Cell and Gene Therapy (CGT) in Boston, Cambridge, and Providence.
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Deep expertise and industry experience in cell therapy process development principals including DOE and experience with current technologies in PSC process development and manufacturing, particularly scalable stem cell culture systems such as bioreactors.
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Bachelor of Science Degree in a relevant field such as manufacturing engineering, mechanical engineering, chemical engineering, materials science, or aerospace engineering. Responsibilities Draper is seeking a product engineer with experience in transitioning electro-mechanical products to manufacturing.
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ADVANCED (OR PREFERRED) QUALIFICATIONS: Experience in gene therapy, particularly formulation and manufacturing of lipid nanoparticles and viral capsids-based drug product is a significant plus Advance knowledge and experience in using chromatographic and biophysical techniques is an added benefit Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce.
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The candidate is expected to have a good understanding of different thin film deposition techniques and semiconductor manufacturing. Ability to handle time sensitive projects and act with strong sense of urgency in a 24x7 manufacturing environment.
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Proven record of process improvement, lean manufacturing, plant and equipment layout, work simplification and methods improvement (Six-Sigma experience a plus). Manufacturing Engineer Job Description ·Refine and enhance processes by applying Continuous Improvement and Lean manufacturing techniques to areas of production.
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Going beyond the existing plant-based burgers, we are developing alternative meat whole-cuts using innovations in materials science, manufacturing and even tissue engineering. Proven track record of developing novel processes, designing experiments to define QA/QC parameters for setting a process envelope, and scaling processes to support manufacturing capacities.
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The Senior QC Analyst position interacts regularly with TScan's Quality Assurance, Analytical Development, Process Development, Manufacturing, Facilities, as well as TScan's external test laboratories, where applicable.
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With one of the largest multimedia air and land permitting and compliance teams in the country, we support client success in manufacturing and industry, liquids delivery and processing, natural gas storage and delivery, power generation and delivery, and transportation projects.
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Vestas is the world's largest wind turbine manufacturing company with significant operations in the United States. Construction Cost Analyst As a Construction Cost Analyst, you will support Offshore Wind Turbine Sales, specifically Construction Costing through the entire sales process from early engagement to contract signing.
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Requirements Requires an advanced degree in Pharmaceutical Sciences, Chemistry, Materials Science, or related field with 5+ years of experience in process development and manufacturing of peptide and oligonucleotide APIs including PMOs. Experience with solid phase peptide/oligo synthesis preferred.
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Experience within a regulated environment, GMP manufacturing environment and with Process Improvement approaches (Lean Manufacturing, Six Sigma, Practical Process Improvement, etc.
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Partner with CMC Regulatory and SMEs to assess compliance with regulatory guidelines and industry best practices for US and EU markets to ensure appropriate quality processes and procedures are implemented for commercial cell-therapy GMP manufacturing, at-scale and in-compliance.
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Deep understanding of drug discovery, development, and manufacturing processes. This is a customer-facing, customer-centric role and requires deep understanding of data management and flow in one (or more) scientific domains including process development, analytical chemistry, CMC, MAbs discovery, lab automation, protein production, in vitro screening, or assay development.
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lean manufacturing jobs Title: buyer Company: Dispensing Systems in Cambridge, MA
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