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Experience in a regulated industry (cGMP, SOPs, audits, etc.) QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine.
$49,500 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Working knowledge of safety and standards guidelines such as SOPs, cGMP, GLP, and DEA regulations. Follow all safety guidelines, including SOPs, cGMP, DEA regulations, and MSDS. Activities include buffer/solution preparation, standard preparation, and operating analytical instruments such as HPLC, UV-Vis, FT-IR, GC, and others.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Must acquire a working knowledge of current Good Manufacturing Practices (cGMP) and ISO requirements. The Chemical Operator works a rotational schedule to meet maintain 24-hour operation of the manufacturing processes.
$47,840 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Must wear appropriate garments and coverings per cGMP (uniforms, hair/beard nets, etc. Executes all packaging processes while strictly adhering to cGMP, Standard Operating Procedures, documentation protocols, environmental health and safety guidelines and any other related regulations that could apply.
Full-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Objective: Safely Operate highly automated and technical equipment and machines in all phases of the contact lens manufacturing process in accordance with all standard operating procedures and cGMP/FDA regulations and requirements.
$24 an hourPart-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Demonstrated experience in the management of the quality and compliance elements of biologics manufacturing activities, applying an intimate knowledge of FDA cGMP and GLP regulations to the manufacture, laboratory testing, and release and testing of biologic drug substances and drug products.
$150,000 a yearFull-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Manufacturing Knowledge: Experience in manufacturing processes is highly valued, especially in regulated industries such as FDA and cGMP. Manufacturing Knowledge: Experience in manufacturing processes is highly valued, especially in regulated industries such as FDA and cGMP.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Working knowledge of eQMS (Quality Systems) and FDA, cGMP regulations preferred. Experience with 3D modeling software (Inventor, SolidWorks, CREO) Experience with process technologies including precision part handling, assembly, vision inspection, laser marking, robotics (Staubli), Allen Bradley/Siemens PLCs.
$91,122 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Acquire and maintain knowledge of cGMP and ISO requirements. Basic computer knowledge in Windows and working knowledge of cGMP. Join Kelly® Professional & Industrial, as a Production Assistant, in Rochester, NY and seize the opportunity to expand your skills while contributing to our team's success.
$21 an hourFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Preferred: Experience in a cGMP environment. A choice of national medical and dental plans, and a national vision plan, including health incentive programs. Monitor, procure and maintain label and printing supplies inventory inside the Label Room as required.
$33.05 an hourFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Follows all cGMP, SOPs and change management requirements and works in a manner consistent with company, regulatory, quality, safety and sanitation guidelines. Experience working in a regulated or FDA cGMP environment is preferred.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines. Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines.
$19 an hourFull-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Supports PET (Positron Emission Tomography) manufacturing sites as needed (manufacturing products, quality control, radiation safety program, cGMP program, Environmental Health and Safety (EH&S), etc.
$93,500 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Our Science, Technology, and Industry (ST&I) Practice undertakes diverse projects in pharmaceuticals, biotech, cell and gene therapy, cGMP facilities, cleanrooms, and various other industrial sectors.
$120,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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We are seeking a Quality Assurance Technician to join our growing biopharmaceutical company and assist in opening our newest Donor Center. One (1) year work experience in biologics quality assurance preferred.
Full-timeExpandApply NowActive JobUpdated 1 month ago
cgmp job in Rochester, NY
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