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Resilience.com Position Summary: We seek an experienced Analyst, QC Bioassay / Biochemistry to support establishing new commercial-level in-house GMP testing laboratories performing release and stability testing for multiple stages of our gene therapy and immune oncology products.
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Analytical Chemist" , Chromatography , HPLC ,MDI , "Metered Dose Inhaler" , DPI , "Dry Powder Inhaler" ,GMP , "Good Manufacturing Practice. Experience working in a GMP testing laboratory, and/or familiarity with relevant external guidance documents and cGXPs in support of analytical testing.
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Tutor Durham Tech students referred from GMP& SOP and BioWork classes or student walk-in; Requested hours specific for GMP & SOP BioWork tutors: approximately 5-10 hours per week. The tutor for BioWork should have overall competency in the following topics:Biotechnology/BioManufacturing/Biopharma Industry PracticesWorking SafelyPharmaceutical Quality Current Good Manufacturing Practices (cGMP)Standard Operating Procedures (SOP)Measurements, Metrics, and MathChemistry for Process ManufacturingProcess Flows, Technology, and EquipmentControlling the Process and Maintaining QualityCleanroom Gowning and Aseptic ProcessingFermentation and Cell Growth.
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Escort outside vendors/contractors such as Pest control, Water treatments, HVAC services, Electricians, Elevator services, Roofers, Document shredding, Recycling services, Custodial services and maintenance services in GMP area, etc.
$16.27 - $24.4 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Demonstrated background in support of GMP Quality management systems, Background in one or more specialties of biotechnology: bioprocess, cell technology, biomedical engineering, cell therapy, tissue engineering, regenerative medicine, process development, cell biology, chemical engineering, and/or biochemical engineering.
$80,000 - $81,000 a yearFull-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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This position will be involved in bioprocess development and GMP production, including lab scale process development; scale up and tech transfer of the process into the GMP suite, and execution of the process under GMP compliant conditions.
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The GMP, Scientist I will contribute to the development, tech transfer, and GMP. development; scale up and tech transfer of the process into the GMP suite, and. involved in bioprocess development and GMP production, including lab scale process.
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Keywords : Microbiology, Microbiologist, QC, Endotoxin, Environmental Monitoring, cGMP, GMP, pharmaceutical manufacturer, manufacturing, Aseptic Manufacturing, Microbiological Laboratory Operations, regulatory, Utility Monitoring, environmental sampling, EM Plates, TOC analysis, Conductivity, Biological Indicators, KTA LAL, Bioburden, Growth Promotion, Micro-IDs, Gas Testing, LIMS, SAP, Trackwise, Investigations.
$30 - $35 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Marken offers a state-of-the-art GMP-compliant depot network and logistic hubs for clinical drug product storage and distribution worldwide, and supports cell and gene therapy logistics services from clinical to commercial, while maintaining the leading position for Direct-to-Patient and Home Healthcare services, biological sample shipments and biological kit production.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Responsible for Fermentation control Systems specific to areas of Seed and Production Fermentors and supporting tanks, supporting YSI, Raman, and Mass Spec equipment, supporting Bulk Chemical equipment, implementations of process change control, Delta V Network and troubleshooting in compliance with system life cycle (SLC), GMP, Data integrity, safety, and environmental regulations.
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Performing routine equipment checks in the Protein Purification Facility and GMP facilities. SENIOR GMP LAB ASSISTANT Duke Human Vaccine Institute The Senior GMP Lab Assistant will be responsible for ensuring the GMP suites are cleaned in accordance to approved Standard Operating Procedures (SOPs.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The downstream manufacturing associate will participate in the purification areas for a clinical and commercial GMP biopharmaceutical facility. Execute daily production tasks to ensure schedule adherence while maintaining a successful and GMP compliant execution.
$33.65 - $45.67 an hourFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Oversee GMP compliance within cleaning, disinfectant, safety equipment inspections, work orders and pertinent tasks utilizing the client’s Computerized Maintenance Management System (CMMS) The Quality Assurance Specialist will be responsible for coordinating and managing project tasks in the GMP Program to ensure project delivery within allotted budget and timelines.
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Experience working in a clean room or GMP/regulated manufacturing environment. Working knowledge of regulatory requirements in accordance with GMP manufacturing operations. The Senior Instrumentation/Calibration Technician will use computerized systems such as SAP, ProCal, PAS-X, DeltaV, and BAS for PM data entry, report generation, and equipment data analysis.
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The Sr. Manufacturing Associate I/II – Upstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment. Additionally, must ensure all work is conducted following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP); including ‘Right the First Time’ (RFT.
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gmp job in Durham, NC
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