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Trains manufacturing and QC/QA personnel on cleaning validation documentation. Provide technical support to cleaning activities associated with the manufacturing process. Design and develop cleaning validation protocols for products and manufacturing equipment, including steaming studies.
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Complete your profile and start locki Forklift Operator, Lift Operator, Forklift, Operator, Staffing, Manufacturing. Complete your profile and start locki Forklift Operator, Lift Operator, Forklift, Operator, Staffing, Manufacturing.
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The Quality Control Analyst is responsible for performing microbiological/analytical test methods on in-process intermediates and varying stages of drug products under minimal supervision and within cGMP guidelines, to support further manufacturing of commercial and clinical therapeutics.
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Gibson operates via a central headquarters based in Nashville, TN, supporting five manufacturing facilities as well as four regionally-based support centres that enable the sales, marketing, and distribution activities in each of four different worldwide regions.
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Knowledge of biotech manufacturing process and equipment including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation and/or buffer and media operations.
$28 - $32.2 an hourFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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One of our top clients in the manufacturing industry is looking to hire an experienced Process Technician Operator to oversee their manufacturing process. As a process technician, you will be working on the factory floor where you will monitor processes, test batch quality, maintain equipment logbooks, ensure the area is clean, and report any machine faults to your supervisor.
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Experience in poultry processing/manufacturing environment preferred. Experience in poultry processing/manufacturing environment preferred. Occasional exposure to carbon dioxide vapors 10ppm and chlorine less than 20 ppm.
$19.5 - $22.95 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.
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Coordinate CMC portfolio plans with global company plans, internal manufacturing site production plans, contract manufacturing production plans, clinical development plans, CMC regulatory filings Focus on continuous improvement of team capabilities by ensuring that partner team leads have the opportunity for training and development to excel in their role as functional representatives and cross-functional team members.
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The Novato campus is home to four commercial manufacturing facilities and a pilot plant facility. The Purchasing Manager must foster a close working relationship with multiple departments at a local level, such as Inventory Control, Manufacturing, Quality, Scheduling, Warehouse Operations, Procurement, and Finance.
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Knowledge of biotech manufacturing processes and equipment including cell culture, depth, and tangential flow filtration, column chromatography, protein purification, and formulation, and/or buffer and media operations.
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Other continuing education initiatives are highly desirable (e.g., Six Sigma, Lean Manufacturing, industry specific coursework). Minimum of 5 years of experience in the biotech/pharma industry with experience in supply chain, warehouse operations, and/or manufacturing operations.
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Comfortable working in a manufacturing environment, including the cheese and yogurt production areas. Experience in a manufacturing background while supervising 12+ workers is preferred.
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Perform daily environmental monitoring sampling of GMP facilities cleanrooms (Galli and Leveroni manufacturing areas) and utility systems (RODI/WFI/Steam water systems and CDA/process gases.) The QC Microbiology department is responsible for performing environmental monitoring and microbiological test methods on in-process intermediates and varying stages of drug products under minimal supervision and within cGMP guidelines, to support further manufacturing of commercial and clinical therapeutics.
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BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. Senior Associate, Quality - On-Site Grave and Weekend Shift.
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manufacturing job in Petaluma, CA
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