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Responsible for directing, coordinating, creating, and evaluating the activities of the Quality Department across Drug Manufacturing (GMP), Clinical Research & Development (GCP), and Pharmacology & Toxicology (GLP) functional activities.
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Responsible for completing paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures. Assist in the execution of procedures for microbial manufacturing, purification, or support area of manufacturing using SOP's and batch records.
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Secondary duties include, but are not restricted to, upgrading and installation of new equipment, electrical, welding, machining, mechanical, etc., while maintaining the highest safety, quality, cost and GMP standards in a high-speed manufacturing environment.
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Tasks are to be completed while maintaining the highest safety, food safety and quality, cost and GMP standards in a high speed manufacturing environment. Assist the Retail Store Manager as needed in the overall operation of the Tea Shop.
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We are seeking a passionate and capable Senior Bioprocessing Associate to support Manufacturing Operations during the startup and operations of our newly constructed early-stage cell/gene therapy GMP manufacturing facility located in Louisville, CO. This role will support routine Manufacturing Operations and primarily be focused on the Upstream steps of our process, however, could be expected to support other manufacturing functions as well.
$36.57 - $44 an hourFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Operate and maintain the high purity water system including the batching and tank cleaning to support the continuous supply of saline and heparin to the manufacturing operations. Must follow GMP guidelines, perform re-qualifications, with related documentation and maintain the proper change control process.
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Ability to understand and apply GMP regulations as they relate to manufacturing, test laboratory and facility operations. AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way.
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Proficient in building and maintaining Global Food Safety Initiative such as SQF or BRCGS. Proficiency in food safety quality system manufacturing processes, quality assurance principles, food manufacturing, SPC, and electronic QMSs (e.g. SAP QM, NetSuite QM, TrackWise, RedZone, SpecRight.
$180,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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This position is also responsible for understanding related Quality Management Systems including SQF, HACCP, and GMP to ensure safety and quality of products. BS degree or equivalent experience in a food manufacturing environment.
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The purpose of the lead maintenance mechanic is to troubleshoot, repair and perform predictive and preventative maintenance of packaging, milling, and blending equipment. Ensure that all paperwork including daily end of shift reports, inventory, safety sheets (ex: hot work permits, confined space) and supply requisitions are accurate.
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Conducts analysis associated with clinical and commercial under current Good Manufacturing Practices (GMP) regulations and guidance per Food and Drug Administration (FDA) and Organization for Economic Co-Operations and Development (OECD) as well as International regulations.
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