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The Assistant/Associate Scientist is responsible for performing analytical testing using a variety of cellular and/or molecular biology analysis platforms. AmplifyBio brings decades of experience to accommodate a wide variety of GLP and non-GLP studies in all in vivo models and dose routes.
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Adhere to principles of GLP/GCLP applicable to bioanalytical sample testing, data analysis and reporting. Provide technical guidance and mentoring to bioanalytical testing staff and other team members as needed in the execution of bioanalytical projects as well as GLP/GCLP best practices.
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The Study Technician provides primary care to the animals in the small and large animal toxicology department and performs routine invasive and non-invasive technical procedures on studies allocated to the team while ensuring that procedures are conducted according to protocol, SOP requirements, Good Laboratory Practice (GLP) and United States Department of Agriculture (USDA) regulations and the guidelines The Guide for the Care and Use of Laboratory Animals.
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Experience with protein characterization, including peptide mapping and intact mass by LC/MS. Experience with HPLC, CE, icIEF, Empower software, Analyst software, Unifi software, Protein characterization, Peptide mapping Compliance with, and knowledge of, regulatory guidelines and company SOPs (CGMP, GLP) is required.
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As a Study Director, you’ll be the single point of control for assigned studies, responsible for the interpretation, analysis, documentation, and reporting of study results for both GLP and non-GLP studies.
$110,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Collecting and reviewing data in accordance with the Good Laboratory Practice Regulations (GLP) and standard operating procedures. Here, you can apply your scientific curiosity in Biology, Animal Science, Zoology, Animal Behavior, Veterinary Technology, Dairy Science, Equine Science or similar majors to pursue advances in animal welfare and research the effectiveness, safety and toxicity of drugs in early development animal research studies.
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As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries.
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Assisting as necessary with the internal GLP activities to conform with the GLP regulations (21 CFR Part 58) across the Medical Device CommunityMaintaining a copy of a master schedule sheet of all nonclinical laboratory studies conducted at Ethicon indexed by test article and containing the test system, nature of study, date study was initiated, current status of each study, identity of the sponsor, and name of the study director.
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Responsible for in-house GLP/GCLP infrastructure, hands on troubleshooting, systems and procedures to ensure adequate rigorous laboratory practices & regulatory requirements for bioanalytical activities assuring phase appropriate approach.
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Job Summary: The Clinical Laboratory Scientist handles all hematology, coagulation, routine chemistry, immunoassay testing with a goal of providing 100% accuracy when processing samples. Performs all essential functions such as laboratory safety, Good Documentation Practice (GDP), Good Laboratory Practice (GLP), specimen processing and troubleshooting, maintaining productivity and quality assigned metrics, and providing effective communication with laboratory management and team.
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Support CGT projects by producing injectable forms of cell-gene therapy products for in-vivo testing. In this dynamic role, you'll be at the heart of our formulation, fill, and finish activities, playing a key part in preparing a wide range of test articles for both non-GLP and GLP preclinical studies.
$25 - $30 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Thorough working knowledge of industry regulations, FDA and ICH guidelines; experience implementing and maintaining adherence to pharmaceutical and/or nutritional supplement GLP/GMP is strongly desired.
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Define and implement analytical testing strategies for BMS Cell Therapy development organization. Leading a team, collaborating with cross-functional stakeholders, and driving strategic decisions related to analytical testing, instrument standardization, tech transfer, and process development.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Our Talent Acquisition team is reviewing applications for our Pulmonary Function Testing Respiratory Supervisor opening. We are looking for a dedicated Pulmonary Function Testing Respiratory Supervisor like you to be a part of our team.
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Job Title: FX QA Manual Testing. 10 years hands on experience in Software development life cycle, preferably in Manual Testing of multi-tiered applications. Integration testing experience with upstream/downstream systems.
$110,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday
glp testing jobs Title: analytical Company: Valentine Enterprises Inc
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