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Learn and maintain thorough familiarity and compliance with all state and federal regulations, Standard Operating Procedure Manual, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP), and internal Company Procedures.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Assist the Manager of Quality Assurance with compliance of all state and federal regulations, FDapproved Standard Operating Procedure Manual, Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP), Occupational Safety and Health Administration (OSHA), and internal company procedures.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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At least 2-4 yrs working experience in a cGMP Quality Control, analytical development, analytical transfer or validation department in a FDregulated industry. Must be able to handling of laboratory equipment, chemicals, and biological materials.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Sr. Associate Compliance provides scientific support in the root cause analysis and closure of OOS investigations, OOT investigations and product quality complaints; ensures compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP) and Quality Management System standards, compiles monthly Quality metrics for internal and corporate review, and analyzes trends to implement corrective and preventive actions to mitigate adverse trends.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Perform laboratory activities including weighing, transferring, and mixing required chemicals and performing product filtration. You will be responsible for manufacturing products for the Bulk Formulations TDM team and complete associated cGMP documentation.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, and cGMP regulations. Use moderately complex laboratory instrumentation (tensile tester, microscope, force gauges, etc.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Creates and issues audit report for each audit to submit to BIVI management to ensure SOP(s), facilities, systems, processes and studies conform to applicable cGMP, Good Laboratory Practices (FDA, USDA, EU), Good Clinical Practices (FDA), and/or Guidance Documents (FDA, USDA, EU) internally and for external contract manufacturers, laboratories, and suppliers.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Laboratory, Food science, Gmp, Cgmp, Chemistry, Microbiology, Fda, Biology. Operate milk laboratory equipment, including but not limited to the following: Foss FT1 component analyzer, Celsis Innovate CellScan analyzer, pH meter, autoclave, refractometer, analytical scales, incubators, 3M petrifilm, etc.
$21 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Expertise in Quality Systems and cGMP standards applicable to method validation for clinical and commercial products and AO/QC laboratory operations. May assist with cGMP compliance audits at contract partners and may interface with regulatory agencies during inspections.
$55 - $65 an hourExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Minimum 3 years of laboratory experience in nutraceutical/pharmaceutical/cosmeceutical. Working knowledge of applicable safety and standard guidelines such as SOP, cGMP, GLP, and MSDS. Assists in laboratory equipment qualifications, calibrations, and preventative maintenance programs.
Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Chemistry Analyst I will work under direct supervision or be partnered with an experienced analyst to perform wet chemistry analyses, preparation of reagents, standardization of solutions, and instrumentation testing and documentation in a cGMP environment.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Experience in one or more functional areas such as quality control, quality assurance, laboratory, manufacturing, production, equipment/facilities management, regulatory. Responsibilities include the following activities: product release, quality system, compliance, document management, and any related activities needed under current Good Manufacturing Practice (cGMP.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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As a Manufacturing Technician II, You will execute all processes in production while strictly following cGMP, environmental health and safety guidelines and any other related regulations which could apply.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Understanding of laboratory equipment such as ddPCR, qPCR, UPLC/HPLC, ICP-MS, UV/Vis Spectrophotometer, Densitometer, Gel Imager, pH, Osmometer, Cell based methods, Microbiology methods, etc. Ensures that internal and external laboratories comply with cGMP standards.
$112,800 - $169,200 a yearExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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For the Senior Validation, Engineer level: Working knowledge of target systems, including computerized information systems, manufacturing control systems (e.g., PLC, BMS, DCS, and SCADA systems), and laboratory automation systems (e.g., robotic systems, chromatography networks, data acquisition systems.
Full-timeExpandApply NowActive JobUpdated 1 month ago
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