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Support technical problem-solving for issues pertaining to GMP Quality Control. Perform daily GMP Quality Control laboratory testing activities at the facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
$45 an hourExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Develop a Subject Matter Expert (SME)-level understanding of and be able to skillfully execute as well as troubleshoot Iovance’s GMP cell therapy manufacturing process(es). Minimum 2+ years of experience in biopharmaceutical-based GMP manufacturing operations, including experience in cell culture and associated downstream processing.
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BMS, SCADA and DCS design, commissioning and validation in GMP facility. Interface with IT to ensure GMP compliant integration with Corporate IT infrastructure. Experience with critical utility and non-GMP utility systems a plus.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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3+ years of experience in the pharmaceutical industry within a GMP Quality Control role; experience with cell therapy products is a plus. Minimum of 2 years experience in the pharmaceutical industry working in a GMP quality control laboratory.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Savour unparalleled fine-dining by Michelin-starred Chef Jean-Georges Vongerichten and inventive flavours by local James Beard Award-winner Chef Greg Vernick. The role of the In-Room Dining Server.
Part-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Abzena, a Partner Research Organization (PRO) for biopharmaceutical outsourced solutions from concept to clinic and into GMP manufacturing, has announced the appointment of Anu Bansal as Senior Director of Manufacturing at its facility in Bristol, Pennsylvania.
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Ability to wear personal protective equipment (bump cap, hair net, ear plugs, beard net (if applicable), Kevlar gloves, safety glasses and leather, skid resistant work shoes/boots. Monitor thermal process checks including pasteurizer temps and packaging sterilization processes.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Four Seasons is partnered with Michelin starred chef Jean-Georges Vongerichten, James Beard award winning chef Greg Vernick and renowned florist Jeff Leatham to create an extraordinary experience.
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Goldie and its 10-year old sister restaurant, Zahav (which means "Gold" in Hebrew), are co-owned by the James Beard Award-winning duo Chef Michael Solomonov and Steven Cook, who have arguably put Israeli cooking on-the-map in the US.
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Thorough understanding of clinical drug development, GMP, GCP, and familiarity with regulatory (FDA, Health Canada, and other global regulations) requirements for the conduct of clinical trials, including investigator-initiated studies.
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The Quality Control Analytical Scientist II will develop, qualify, and perform analytical methods that are used to test and characterize GMP Raw Materials, In-Process Samples, Drug Substance and Drug Products.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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The Executive Chef must have Michelin Star or James Beard Pedigree. The Executive Chef is responsible for all kitchen operations with an emphasis on production, supervision of all stations, catering and menu development, and will work closely with the Catering Chef and Catering Director.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Demonstrated working knowledge of design controls, analytical, clinical, and manufacturing process validation requirements for IVDs, GCP, GLP, and GMP requirements; working knowledge of requirements for US and global regulatory submissions related to IVDs for use in clinical trials and for commercialization of companion diagnostics.
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B.S. degree in Engineering, Chemistry, or related scientific discipline plus a minimum of 8-10 years of experience in pharmaceutical product transfer, process development, technology transfer and validation, and/or process engineering for injectable products in a GMP environment.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Minimum 1 year experience working in a clinical or research lab or equivalent GMP/GLP setting (Required). Minimum 1 year experience working with tissue culture techniques, flow cytometry and/or molecular biological assays (Preferred.
Full-timeExpandApply NowActive JobUpdated 1 month ago
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