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Prefer Operational Excellence experience in a regulated industry such as pharmaceutical, nutraceutical or food processing industries, with familiarity of cGMP and other regulatory requirements.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Responsible for operating Simplex & Kalix production equipment in accordance with established SOP's (Standard Operating Procedures) and cGMP (current Good Manufacturing Practices) guidelines. Responsible for operating Simplex & Kalix production equipment in accordance with established SOP's (Standard Operating Procedures) and cGMP (current Good Manufacturing Practices) guidelines.
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Provide cGMP and associated OJT training to QA and other departments to improve right the first time (RTFT) initiatives, high quality performance. Complete job-related training in electronic database system along with GMP, safety, and Ethics & Compliance course requirements.
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Knowledge of established Quality Systems, ISO regulations and/or cGMP. The Staff Scientist is responsible for crafting and leading projects for insourcing/outsourcing changes of processes, raw material and/or finished goods for the Chemical and Biological commodity.
Full-timeExpandUpdated 9 days ago - UpvoteDownvoteShare Job
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Maintain cGMP supplies such as hairnets, ear plugs, and beard nets. Maintain cGMP supplies such as hairnets, ear plugs, and beard nets. Communicate with the lead person as to specific job requirements.
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5-10 years of relevant project management experience related to laboratory use, laboratory construction projects, operational and/or design experience in biology, chemistry, vivarium, cGMP and/or clinical diagnostic laboratories.
$120,000 - $150,000 a yearExpandUpdated 12 days ago - UpvoteDownvoteShare Job
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The position will work with Quality to assist in maintaining cGMP compliance for products manufactured, packaged, tested and released. Getinge is seeking an intern to work in the supplier quality team for Cardiac Surgery division.
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Drugs, biologics) and ex-US requirements ensuring ongoing compliance with FDA/ICH regulations, guidelines and current Good Manufacturing Processes (cGMP). drugs, biologics) and ex-US requirements ensuring ongoing compliance with FDA/ICH regulations, guidelines and current Good Manufacturing Processes (cGMP.
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The engineer will perform a wide variety of tasks following cGMP which will include the. SkySys specializes in Recruitment & Staffing, 24/7 On-Site & Remote Services, Managed Services Provider (MSP), Value Added Reseller (VAR) partner for Cisco and Dell, Contact Center Solutions (Cisco, Avaya, Genesys), Web Solutions, and other services.
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Required Experience: Minimum of 2 years of Project Management and Operational Excellence experience in a regulated industry such as pharmaceutical, nutraceutical, food processing or highly regulated industries, with familiarity of cGMP and other regulatory requirements.
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Ensure all materials/reagents are accepted according to SOPs and within expiry Ensure all equipment is appropriately qualified prior to use Ensure completion of applicable cGMP documentation. Requirements: Bachelor’s degree in chemistry or a related science field Experience with analytical instrumentation such as HPLC or GC-MS is a plus.
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Education & Experience: Two or more years of experience in pharmaceutical, dietary supplement or food industryExperience cleaning equipment Knowledge of cGMP regulations and experience in cGMP environmentHigh school diploma or GED with relevant experience.
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KDC is a network of best-in-class custom formulators and manufacturers of color cosmetics, skincare, haircare, bath & body, fragrance, deodorant, home, health, industrial, and auto care products. KDC delivers high-touch innovation, operational excellence, and speed to market to well-known and emerging beauty, personal, and specialty companies from coast to coast.
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Assist Center Manager in ensuring all center operations, product storage, documentation, facility maintenance, quality control, and training is current and consistent with the Company's Standard Operating Procedures Manual (the "SOP"), current State and Federal guidelines, OSHA, CLIA, cGMP, and any other internal Company procedures.
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Currently a junior or senior student attending a 4-year undergraduate program, or working towards a Master's degree in a related life science field. At Getinge, our passion is to secure that every person and community have access to the best possible care, offering hospitals and life science institutions products and solutions that aim to improve clinical results and optimize workflows.
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cgmp job in Fairfield, NJ
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