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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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In health, we focus on areas like medical countermeasures, advanced therapeutics, regenerative medicine, cell and gene therapies, biologics manufacturing, natural products, APIs and KSMs, enzymes, biocatalysis, and microbiome therapy to support national health security and public health initiatives.
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Machine Learning | Semiconductor Manufacturing | AI | Electrical Engineering | Automation | MLOps | Java | C. Lead the development and deployment of machine learning algorithms for semiconductor manufacturing challenges.
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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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Director/Sr. Director - Process DevelopmentGreater Boston Area Competitive Compensation + excellent bonus/benefitsDuties and Responsibilities:Lead all process development activities (cell culture/banking/development, fermentation, protein purification, tech transfers)Oversee internal(in-house) and external vendors (domestic & international CDMOs)Work cross-functionally with CMC & Manufacturing leaders such as Analytical, Drug Product, QA/QC, Manufacturing, Supply Chain, etc.
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E.g. Allen Bradley, Siemens and CODESYS systems- Experience with the designs of complex, automated material handling equipment, packaging technologies, or systems including robotics (FANUC, ABB, UR) and high-speed manufacturing.
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Bachelor's degree in technical discipline (Biology/Chemistry/Microbiology/Engineering or related field) with a minimum of 3-5 years of experience in Quality Assurance, Quality Control, or a GMP related field within a biotechnology, biologics, or pharmaceutical manufacturing facility.
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This position leads various teams within FMI, directing quality personnel working with manufacturing and IVD operations teams within the Quality System Program, including manufacturing process review, batch release of products, IVD assay validation and verification, manufacturing material acceptance, device non-conformance and CAPA investigation.
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Knowledge of biotechnology/pharmaceutical product development process including technical transfer, manufacturing, process development and characterization, analytical/assay development, regulatory filings, and clinical/commercial operations.
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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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Tecogen Inc. has an immediate opening for a full time Engine Mechanical Assembly Technician located in Waltham, MA to work in our manufacturing facility. Manufacturing Technicians are provided will all necessary tools.
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If you are interested please send a MS Word version of your resume to me or if know of someone that would be a great match, please have them contact John Marino at Source Recruitment Solutions John@SourceRecruitmentSolutions.com Or simply apply now by clicking the "APPLY NOW" link: #maintenance #industrialMaintenanceMechanic #manufacturing #PLC #LadderLogic #MaintenanceMechanic #Maintenancejobs #ZR #ZipRecruiter #Monster.com #jobs #Mechanic #LinkedIn #simplyhired #hiring.
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We are seeking a passionate Research Associate II/Senior Research Associate to work in the Protein Engineering and Molecular Sciences Team to support analytical and biophysical QC of TCR bispecifics and MHC proteins as well as development of analytical assays for tech transfer to manufacturing.
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Support the planning and implementation of manufacturing process development, scale-up, technology transfer, and validation efforts in API, drug product, and primary packaging, ensuring strategic alignment and operational excellence.
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10+ years of experience in cGMP biologics, cell therapy, or vaccine manufacturing. The Director, Cell Therapy Manufacturing is responsible for the leadership, oversight and strategic planning required to support the key business needs of all Cell Therapy product lines manufactured by Vericel.
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manufacturing job Company: Gpac in Boston, MA
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