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Conduct a specific micro testing under guidance of the microbiologist. Adhere to and models good manufacturing practices (GMP) and good laboratory practices (GLP) at all times. Obtain samples from production and process sample preps for micro testing, including media prep as directed or outlined in the protocol.
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Review early-stage analytical testing in support of GLP and GMP clinical protocols and production activities. Review of GMP/GLP documentation from manufacturing and/or Analytical Operations, which can include logbooks, and test records.
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Responsibilities:Responsible for GLP, including equipment monitoring and calibration as well as media preparation and biohazard disposalEvaluate, develop, implement, and maintain testing procedures and programs.
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Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP.
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Experience and knowledge in the pharmaceutical sampling and testing of critical utilities and environmental monitoring within a GMP and/or GLP environments preferred. + Cell Culture Experience highly preferred + cGMP or regulated manufacturing or testing experience preferred + Experience performing USP (United States Pharmacopeia) compliant testing preferred.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Certified Group includes Food Safety Net Services (FSNS), Certified Laboratories, EAS Consulting Group, Labstat International Inc., Advanced Botanical Consulting & Testing (ABC Testing Inc.), Microconsult Inc., and Micro Quality Labs Inc. Certified Group provides laboratory testing and regulatory consulting services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, tobacco, nicotine, cannabis, hemp, and other industries.
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Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures. Certified Group is a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services.
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Maintains good manufacturing/laboratory practices (GMP or GLP), orderly and accurate paperwork, quality systems, and maintaining the integrity of manufactured product. May use statistical methods and programs to analyze data from experiments, QC testing results and other data.
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Perform analytical and microbiological testing of food products, ingredients, and environmentals. Two or more years of experience in a commercial food-testing or analytical laboratory. Broad knowledge of concepts, practices, and procedures of a food testing laboratory.
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1+ year of previous experience from a GxP facility, particularly in conducting clinical drug safety assessment testing in in vivo test models, including sample collection, processing, and basic analysis.
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Report inventory and expendable supplies/materials needed for testing requirements. We are currently looking for a Pathogen Lab Analyst to join our growing team! Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc.
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Keywords: GMP, GLP, GXP, GCP, batch record management, batch record review, full-process manufacturing, cell therapy, deviations, junior role, maintenance, calibration, FDA, EMA, biopharmaceuticals, quality assurance, QA.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Perform data review on all types of analytical testing performed in the lab, including but not limited to, Identification testing, Wet Bench testing, Titration, HPLC, GC, ICP-MS, etc.
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The QC Analyst will set up and execute daily testing of final API product and raw materials. Minimum: 2-4 years of experience in a cGMP/GLP laboratory with experience operating analytical instrumentation.
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We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development.
ExpandApply NowActive JobUpdated 11 days ago
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