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Centred out of LGC’s site in Kulmbach, Germany, Axolabs works closely with its customers to assist the identification and development of lead candidates with a broad suite of bioinformatics, biology, chemistry, manufacturing and analytical services that support discovery, pre-clinical and clinical trials and scale-up manufacture.
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TITLEQC Microbiology AnalystSUMMARYThe QC Analyst 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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Essential Responsibilities:Must be able to perform the typical duties of a Pharmacist such as manufacturing, dispensing, maintaining control of drugs and pharmaceuticals supplies, and performing other related work as required.
$36.76 - $38.68 an hourInternExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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BS/BA in a scientific discipline or related field and 6-8 years experience in a biologics manufacturing environment. 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.
$93,200 - $139,800 a yearFull-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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You will leverage market insights, sales data and consumer research to identify white space opportunities and partner with our world-class scientists, herbalists, field experts and technicians in Research and Development, Sourcing, Quality and Manufacturing to lead the development of new products from concept to commercialization.
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Experience Preferred Experience in poultry processing/manufacturing environment preferred. Experience Preferred Experience in poultry processing/manufacturing environment preferred. Occasional exposure to carbon dioxide vapors 10ppm and chlorine less than 20 ppm.
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In-depth understanding and application of cGMP principles, concepts, practices, and standards-Regulatory, Quality, Compliance, or a combination of technical experience such as analytical development/manufacturing sciences and Quality/Regulatory.
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The Oligonucleotide Production Technician I will perform tasks associated with the production of modified oligonucleotides in a high throughput time sensitive manufacturing environment in compliance with company procedures and external regulatory requirements.
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Founded in 1990 and headquartered in Novato, CA, with additional offices in Ferndale, WA, McAllen, Tx, Mundelein, IL; the Company has its product development, manufacturing and 3PL capabilities across the continental U.S. and Canada.
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Experienced Tax Professional Summary Our client is a large full service accounting, auditing and financial services firm servicing its national and international clients through with multiple offices nationally We are known for our reputation for excellence with a variety of specialty areas like agribusiness, nonprofit, research and development tax credits and incentives, employee benefit plan and government audit, manufacturing, warehousing, automotive dealerships, and many more.
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Join our team as a full-time Assembler/Shipping Assistant, where you will be responsible for various manufacturing, shipping, and warehouse support duties. Your role will involve assembling irrigation controllers that help customers conserve water.
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Performs microbiological, biochemical, and chemicalevaluations of the manufacturing facilities, utilities, and equipment. Performs biochemical and microbiological assays ofsamples under cGMP and GLP guidelines.
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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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Protein determination by Bradford and UV Absorbance, Enzyme activity, Endotoxin detection, Bioburden quantification, HPLC, and Total Organic Carbon. Timely facilitation of incoming sample receipt and accessioning flow.
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manufacturing job in Petaluma, CA
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