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Primary activities include but are not limited to the following: Conduct a real-time flow cytometry assay in support of increased manufacturing process control and consistency in viral growth kinetics.
$23 - $25 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The ideal candidate will work with the Head of Process and Analytical Development -Cell Therapy, customers, and internal scientific leaders to design and implement technical strategies which deliver the latest scientific and analytical innovations to our technical development and manufacturing infrastructure, network and client partners.
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Experience with protein drug product manufacturing processes and development (e.g., solution in vial/PFS, or lyophilization); container/closure assessment & selection, drug delivery (e.g., combination product, device & administration kit) feasibility and compatibility evaluation.
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Does this person have experience working on CMC (Chemistry Manufacturing and Control) or Safety/DMPK aspects of pharmaceutical products as a workstream/technical lead? 5+ years of pharmaceutical industry experience in technical CMC (Chemistry, Manufacturing, and Controls) small molecule, biopharm or non-clinical safety/disposition.
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Documented printing and managerial experience in a fast-paced manufacturing environment. Oversee all aspects of Flexo, screen printing operations, RFID; variable data operations, including but not limited to, training, supervision, maintenance, production, scheduling, quality, process improvement, die and roller management, platemaking, screen processing, ink and material management.
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As a Biopharmaceutical Drug Product, Principal Scientist/ Investigator, you will join the GSK sterile Drug Product Development organization and work on developing late phase drug product formulation, manufacturing process and delivery systems for protein-based therapeutics and NCEs.
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People skills skills: SOP, CAPA, GCP (Good Clinical Practice), PMP, GMP (Good Manufacturing Practice) Project management and/or continuous improvement experience or certification such as PMP, CBAP, AIM or Lean Six Sigma Green Belt/Black Belt a plus.
$58.12 - $72.27 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience with manufacturing configuration control, electronic or semiconductor manufacturing preferred. Bachelor’s & 3 years of experience or GED & 7 years in manufacturing configuration control or equivalent.
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5+ years working in a food manufacturing technical or senior management role, preferably in the meat and/or poultry processing industry, with specific experience managing HACCP and SQF programs.
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S/he will lead a team tasked with the integration of new equipment/technologies and approaches to fast decisional analytical outputs to enable decision-making with respect to process development for both lentiviral vectors and cell therapy processes, resulting in transformative cGMP Manufacturing processes with breakthrough COGs.
Full-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Learn specification, design, and configuration of programmable logic controllers (PLC), Emerson DeltaV distributed control systems (DCS), manufacturing execution systems (MES), and data historians (OSI PI.
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Reports any changes in resident's/patient's condition to the Hospice Nurse and, if in a facility, to the facility nurse and documents the information on the Home Health Aide Certification of House form, including the date and time of the report and the person receiving the information.
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Two or more years of experience in Chemistry, Manufacturing and Controls (CMC) regulatory affairs or product development experience with direct involvement in regulatory submission preparation across all stages of development through to early life cycle submissions.
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Knowledge and experience in gene therapy and gene editing in AAV manufacturing are preferred. Reporting directly to the Analytical Development (AD) and Testing Lead, the Analytical Development (AD) and Testing Senior Analyst will support the management of the life cycle of analytical development for in-process, release and stability program testing of raw materials, plasmids, cell/bacterial banks, drug substance and drug products, in support of discovery, development, and manufacturing of iECURE’s product portfolio from the clinic through commercial launch.
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Maintenance, Inspector, Engineer, Technician, Manufacturing, Quality, Engineering, Technology. 3-7 years' experience as a mechanical technician or test technician in a manufacturing or laboratory environment.
$23 - $28 an hourExpandApply NowActive JobUpdated Today
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