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Responsible for supporting the sample management process for QC (pick up from manufacturing, maintaining chain of custody in LIMS, aliquoting/delivering samples to appropriate lab, etc) At a minimum, the individual should be considered able to demonstrate the following: Acts safely and follows all EH&S safety requirements for site and QC laboratories sufficient depth of knowledge within their scientific discipline and previous area of experience good written and verbal communication techniques.
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Process Equipment (e.g., Filling Machine, Bioreactors, Autoclaves, Glass Washers)Utility Equipment (e.g., Chillers, Boilers, Clean steam generators, Water-For-Injection generation/distribution, reverse osmosis skids, compressed gas systems.
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Relevant experience in good laboratory/manufacturing practices (GLP/cGMP), laboratory quality control or stability, and interaction with quality assurance. In this role, you will support a diverse variety of qualification activities for manufacturing processes within a pharmaceutical manufacturing facility.
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Utility Equipment (e.g., Chillers, Boilers, Clean steam generators, Water-For-Injection generation/distribution, reverse osmosis skids, compressed gas systems) Based on our innovative approach to developing genetic medicines, as well as our industry-leading internal manufacturing capability and expertise, we have become the Astellas Center of Excellence for their newly created Genetic Regulation Focus Area. We are currently exploring three gene therapy modalities: gene replacement, exon skipping gene therapy, and vectorized RNA knockdown, with plans to expand our focus and geographic reach under Astellas.
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Analyze plant labor, scrap, operational spending, and inventory transactions for optimal manufacturing levels. Develop Manufacturing site Policies, Procedures, and Internal Controls. Prepare journal entries where necessary and allocation of all Purchase Price and Manufacturing variances.
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Our Co-op program give students opportunities to build on their academic skills and gain valuable hands-on experience in a manufacturing environment. Fall 2024 Manufacturing Engineering Co-Op Intern.
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Benefits: Forklift Operator, Lift Operator, Forklift, Operator, Staffing, Manufacturing. Were seeking Stand-Up Reach Forklift Operators to work at a local cosmetic manufacturer in Sanford, NC! Benefits: Forklift Operator, Lift Operator, Forklift, Operator, Staffing, Manufacturing.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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As an Excavator Operator, you will operate machinery to perform activities such as excavating, backfilling, trenching, ditching, clearing, looming, fine grading, and final clean up. Employee Stock Ownership Program (ESOP) Health, Dental, Group life insurance Prescription drug plan 401k Retirement plan Health Saving Account (HSA) or Flexible Spending Account (FSA) Health Reimbursement Account (HRA) TELADOC Employee Assistance Program Free Wellness Program Paid vacation/Paid time off CONTACT US If you are interested in this Excavator Operator position in Sanford, NC then please APPLY NOW.
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The vaccine manufacturing capabilities center on large-scale microbial fermentation, purification, conjugation and cell banking. This site has flexible, multi-product manufacturing capabilities and facilities focused on testing vaccines intermediates and drug substance, and gene therapy drug substance and drug product.
$30 - $37 an hourFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Responsible for supporting the sample management process for QC (pick up from manufacturing, maintaining chain of custody in LIMS, aliquoting/delivering samples to appropriate lab, etc) Individual should have knowledge of current Good Manufacturing Practices (cGMP), Laboratory Information Management System (LIMS), Microsoft Office applications specifically Word and Excel, analytical techniques and instrumentation, Lean Six Sigma concepts, and Lean Labs.
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Support the execution of the manufacturing roadmap in line with the Central to Home vision, including deep understanding of operational technology solutions (SAP/ERP, CMMS, QMS, safety, data analytics and visualization, process development and implementation, training systems, etc.
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Key responsibilities are performing GMP tasks associated with maintaining compliant Quality Control and Stability laboratories; providing sample management support for QC; and creating, reviewing and approving documentation.
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Minimum 10 years’ experience as an Automation Engineer in a Pharma / Biopharma manufacturing and/or project environment. Knowledge of and experience in Manufacturing Execution Systems (MES) and interface with Enterprise Resource Planning (ERP) Systems.
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Experience with EBR design for Biotech, Gene Therapy, Vaccine Manufacturing, and Packaging processes in Pharma. Experience with EBR design for Biotech, Gene Therapy, Vaccine Manufacturing, and Packaging processes in Pharma.
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Nice-to-HaveExperience maintaining DeltaV libraries in order to support commercial manufacturing. Experience with the manufacturing of monoclonal antibody API materials for clinical (including late stage clinical) and cGMP commercial phases.
$64,600 - $107,600 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago
clean manufacturing jobs in Sanford, NC
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