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Assay development, assay, immunology, Laboratory, biochemistry, immunohistochemistry, glp, gmp, Chemistry, Elisa. Work under Good Laboratory Practices (GLP) at all times, and work under Good Manufacturing Practices (GMP) where required.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Quality Assurance Specialist will perform laboratory inspections, participate in sponsor and regulatory audits, reviews research data and reports, assists in verifying the Institutes compliance with Good Laboratory Practices (GLP) and Institute study protocols, policies and standard operating procedure s.
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Preference will be given to candidates with direct relevant experience in GLP bioanalytical chemistry. Lovelace Biomedical Research Institute (LBRI) is seeking an experienced Research Associate in Bioanalytical Chemistry with considerable experience.
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Regulatory Compliance: In-depth knowledge and ability to ensure compliance with USDA standards, Animal Welfare Act, The Guide for the Care & Use of Laboratory Animals, NIH Public Health Service Policy, FDA GLP regulations, DEA Regulations, AAALAC guidelines, and all relevant state, county, and city rules and regulations.
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Understanding of cGMP/GLP and GDPs practices and EHS requirements of pharmaceutical lab and production environment. We design, supply, and service a range of water systems and monitoring equipment in industries ranging from pharmaceutical to food and beverage applications, and from microelectronics ultrapure water to municipal water and industrial wastewater treatment.
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Study Directors play a crucial role in managing preclinical research in all aspects of drug development as the single point of control responsible for the overall conduct in accordance with Food and Drug Administration's (FDA) Good Laboratory Practice (GLP) Regulations.
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GLP Pharmaceutical industry experience preferred Registration as a RQAP-GLP is desired. Work experience in monitoring nonclinical Good Laboratory Practice (GLP) research is desirable.
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Review research data and reports, assists in verifying the Institutes compliance with Good Laboratory Practices (GLP) and Institute study protocols, policies and standard operating procedures. Our client a not-for-profit research institute is seeking a Quality Assurance Specialist to join their growing team.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Superb collaborative opportunities exist with the UNMCCC Consortium partners in high-end technology and advanced material or computer sciences (at Sandia and Los Alamos National Laboratories) and GLP toxicology (Lovelace Respiratory Research Institute.
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Seeking a full-time Quality Assurance Specialist under the general supervision of the Quality Assurance Director. A Post-offer pre-employment physical and background check and the ability to gain and maintain access to Kirtland Air Force Base (KAFB) is required.
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