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Strong understanding of upstream and downstream bioprocessing technologies, including cell culture, purification, and bioreactor systems. Our client is at the forefront of innovation in the biotechnology industry, specializing in upstream and downstream bioprocessing solutions.
$150,000 - $175,000 a yearExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Minimum of 5-10 years of experience in biopharmaceutical based GMP manufacturing operations, including experience in cell culture and associated downstream processing. Preferred Education, Skills, and Knowledge Minimum 3 years of experience in biopharmaceutical-based GMP manufacturing operations, including experience in cell culture and associated downstream processing.
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Experience in cell culture and/or protein purification. Reporting to the Pilot Plant Manager, the Pilot Plant Associate will participate in upstream and downstream areas of AAV development in the Pilot Plant for new gene therapy programs and processes.
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Biology, mammalian cell, cell culture, aseptic technique, cryopreservation, thawing, gowning up, gmp, cgmp, upstream, downstream, mammalian, gene therapy. -High School diploma and over 4 years of relevant experience OR Associates'/Bachelor's (science preferred) degree with over 2 years of relevant or equivalent experience OR Master's Degree with strong academic experience with Cell Culture & Aseptic Technique.
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3+ years of experience in biopharmaceutical based GMP manufacturing operations, including experience in cell culture and associated downstream processing. Develop a Subject Matter Expert (SME)-level understanding of GMP cell therapy manufacturing process(es.
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Basic interactions Manufacturing Cell Culture, Manufacturing Purification, Manufacturing Compliance, Engineering & Technology, Supply Chain, Quality Assurance, Quality Control Does not require extensive technical knowledge of manufacturing operations.
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Experience with mammalian cell culture, production and/or purification desired. Great opportunity to be part of a dedicated team serving the rapidly expanding cell and gene therapy (CGT) market.
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Microbial fermentation and/or Mammalian cell culture in. Bench-scale to Large-scale Chromatographic (AKTA) and HPLC systems (Agilent) Microbial fermentation and/or Mammalian cell culture in.
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Extensive experience with molecular biology techniques as related to cell and tissue culture, preparation of brain samples for downstream mass spectrometry proteomics analyses. Have experience in cell culture and associated aseptic techniques.
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Communicate and collaborate with Cell Culture Development team members and other cross-functional areas (Downstream and Analytical Development). Lundbeck Seattle Biopharmaceuticals (LuSBP) is seeking a highly motivated individual to join the Cell Culture Development (CCD) team as a summer intern, participating in upstream process development for biopharmaceutical products The successful candidate will learn aseptic cell culture techniques, bioreactor operation (250 mL to 200 L), cell culture media preparation, in-process analytical instrumentation, statistical experimental design, and data analysis with JMP Software.
$20 - $22 an hourInternExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Minimum 1 years of experience in biopharmaceutical-based GMP manufacturing operations, including experience in cell culture and associated downstream processing. Minimum 1 years of experience in biopharmaceutical-based GMP manufacturing operations, including experience in cell culture and associated downstream processing.
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They will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing.
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In this vital role you will directly support the execution of cell culture, harvest, and purification process studies using up to 500L scale pilot equipment including Single Use bioreactors, chromatography skids, and filtration systems.
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Just - Evotec Biologics' Bioreactor Process Development group is seeking an enthusiastic and hardworking team member who is passionate about expanding worldwide access to biotherapeutics through the advancement of continuous bioprocessing technology and mammalian cell culture processes.
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Strong knowledge of cell therapy manufacturing processes, including cell culture, cell expansion, gene editing, and downstream processing. As a Senior Director, Manufacturing Data Science and Technology (MDS&T), you will play a pivotal role in leading and overseeing the end-to-end manufacturing, technology transfer and refinement of scalable cell therapy production processes.
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