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The tutor for BioWork should have overall competency in the following topics:Biotechnology/BioManufacturing/Biopharma Industry PracticesWorking SafelyPharmaceutical Quality Current Good Manufacturing Practices (cGMP)Standard Operating Procedures (SOP)Measurements, Metrics, and MathChemistry for Process ManufacturingProcess Flows, Technology, and EquipmentControlling the Process and Maintaining QualityCleanroom Gowning and Aseptic ProcessingFermentation and Cell Growth.
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1+ years of experience within the biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy. Train and mentor new manufacturing associates on procedures, aseptic techniques, equipment and trouble-shooting skills.
$20 - $45 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Support process operations by performing support specific and real time floor service tasks (i.e., kitting and kit cleaning, inventory management and data entry, sample management and data entry, aseptic behavior for cleaning of equipment, and cryopreservation) according to standard operating procedures and batch records, while recording production data and information in a clear, concise format.
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As part of an aseptic, beverage manufacturing facility the Plant Sanitation Technician will be critical to maintaining a clean and orderly production facility ensuring the highest quality standards of sanitization for food production.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Prior experience with cGMP operations or aseptic technique. Eclaro is looking for a Bioprocess Associate for our client in East Syracuse, NY. Familiarity with general chemistry, microbiology, or clean room operations.
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They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. The Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions.
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Ensure timely manufacturing of all liquid parenteral cGMP products using aseptic processing technology to deliver high-quality sterile products to the pharmaceutical industry. Work experience in a sterile aseptic injectable processing environment is preferred.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Strong knowledge of aseptic techniques, cGMP regulations, and quality management systems. Proven experience in aseptic production management, preferably in the pharmaceutical or biotechnology industry.
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Role: Bioprocess Associate – Night Shift. Work is performed in a biologics manufacturing environment with classified areas requiring clean hygiene, specified gowning, and personal protective equipment (PPE.
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Minimum of 8 years of experience as a technical writer, with a focus on aseptic manufacturing processes. As a Senior Technical Writer specializing in Aseptic Processes you will play a critical role in documenting and communicating complex aseptic manufacturing processes and procedures.
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Knowledge of aseptic sampling and testing techniques and microbiological testing according to FDA, cGMP, GLPs and USP testing methodology. Knowledge of aseptic technique and microbiological testing according to FDA, cGMP, GLPs and USP testing methodology.
$23.5 an hourFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The incumbent will be responsible processing human birth tissue in an FDA regulated environment and following all cGMP requirements. Responsible for aseptic processing of birth tissue in a cleanroom environment, including processing area set up and change over as needed.
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Compile and review raw data, batch records and test results, including Final Reports and CoA’s, in accordance with cGMP. Ensure good aseptic processing practice by manufacturing during shop floor support.
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Must possess general knowledge of virology, cell culture laboratories, cell culture husbandry, and aseptic techniques. PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and government agencies.
$101,383 - $124,846 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Experience 3 years of demonstrated relevant experience in performing Environmental Monitoring in a GMP Pharmaceutical Manufacturing facility, preferably associated with aseptic production. Previous experience with Laboratory IT systems such as LIMs, LES, and MODA. Additional Preferences: Experience with cGMP requirements and regulatory compliance associated with a cGMP Manufacturing facility.
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