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Ability to work in compliance with all local, federal, GLP, FDA, USDA regulations. Works in compliance of all applicable local, federal, GLP, FDA, and USDA regulations. Documents in medical records, GLP forms, etc.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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For the Principal Research Scientist I position, we are seeking a highly motivated, experienced analytical scientist and leader to lead a team of analytical scientists supporting the development of New Chemical Entities (NCEs) drug substance and drug product from pre-clinical through Phase III under GLP and GMP guidelines.
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Skills: HPLC, Chemistry, Chromatography, GLP (Good Laboratory Practice), GCP (Good Clinical Practice), GMP (Good Manufacturing Practice) Solid use of instruments including HPLC, GC, MS, UV/VIS, APC. Solid documentation skills, familiarity of GMP, GLP. Able to present findings to larger groups.
$30 - $38.18 an hourFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Experience working in a laboratory with knowledge of GMP, GDP and GLP, and an ability to operate lab equipment with practical and technical knowledge of common lab instrumentation and equipment used for testing, is a plus.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Ensures that complaint documentation meets Good Documentation Practices as well as GMP and GLP. Responsible that complaint data meets all regulatory requirements. Responsible for reviewing complaints that involve a non-medical quality related problem.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Perform all required tests to release reagent products in compliance with cGMP/GLP. Inspect and release incoming raw materials for production use. Keep daily calibration records of laboratory instruments, including pH meters, osmometer, conductivity meters, refractometer, and blank check for Sysmex instruments.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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HS, AS, or BS graduate with some lab experience, GMP/GLP/CLIA is a plus. Previous laboratory experience is preferred but not required, GMPs and GLP. HS, AS, or BS graduate with some lab experience, GMP/GLP/CLIA is a plus.
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Maintains good laboratory practices (GLP) consistent with MDS product development objectives and regulatory guidelines. Particpiate in Equipment and Test Method validations at the direction of the TMD/V&V group.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Strong interpersonal and communication skills+ Preferred:+ Experience in LIMSskills: GLP (Good Laboratory Practice), GCP (Good Clinical Practice), Laboratory Information Management Systems (LIMS), GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management SystemEqual Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Solid documentation skills, familiarity of GMP, GLP, GSP. Solid documentation skills, familiarity of GMP, GLP, GSP. Solid use of analytical instruments including HPLC and chromatography data systems (i.e., Empower.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Familiar with GDP and GLP. Performs a variety of routine and, in some cases, non-routine work as delegated by the lab supervisor or senior technicians. Familiar with GDP and GLP. Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only.
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The R&D technician is expected to comply with procedures set forth in SOPs, GLP guidelines, DEA policies, protocols and/or other directives issued by the Study Director or management regarding non-clinical laboratory studies.
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Minimum 5-8 years of industrial experience in R&D or process development, or Associates degree in science, math or engineering with 4 years related experience preferably in medical device or other regulated FDA/QSR and ISO environment.
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