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Experience with viral infections; cell culture and cell line derivation; nucleic acid (RNA & DNA) extraction from primary human samples; nucleic acid characterization by spectrophotometer, Agilent, and fluorescence-based detection.
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Our newly built, state-of-the-art 40,000 sq ft laboratory opened Q1 2024 and serves as a global center of excellence for gene therapy companion diagnostics, large molecule bioanalytical, immune monitoring, and cell biology assays.
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Ability to apply critical thinking, independent decision-making, high attention to detail, and troubleshooting skills to complex biologics manufacturing, cell culture, and/or cell therapy production issues.
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Background in one or more specialties of biotechnology: bioprocess, cell technology, biomedical engineering, cell therapy, tissue engineering, regenerative medicine, process development, cell biology, chemical engineering, and/or biochemical engineering.
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As a Scientist III,You will play a pivotal role in the development of new products with applications in transfection and delivery of macromolecules such as RNA and DNA, protein delivery, protein expression, and cell culture.
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Demonstrates proficiency in cell culture and in vitro virology and/or toxin assays. Collaborates with other scientific staff to identify and implement continued process improvements to NBTCC cell culture operations.
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Must have either a phone, computer or tablet with either a working camera or webcam Work Education Requirements: - Will vary by study but all education backgrounds are acceptable This is a perfect position for those looking for either temporary, part-time or full-time remote work at home.
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Or from an accredited college or university according to the Council for Higher Education Accreditation (CHEA. Foreign degrees must be evaluated for equivalency Demonstrated expertise in applying experimental methods that are relevant for investigating drug MOA and pharmacology, for example methodology from the fields of cell biology, immunology, genetics, genomics, molecular biology, biochemistry, chemistry, enzymology, pharmacology, drug discovery and/or similar disciplines.
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Perform testing of raw materials, intermediates and final products by following analytical methods: Cell based bioassays, Flow Cytometry, ELISA and qPCR assays. Must have experience in analytical methods: Cell based bioassays, Flow Cytometry, ELISA and qPCR assays.
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The Cell Therapy Specialist will perform and/or verify all tasks associated with the manufacture of commercial product following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations as well as works as part of a team to execute GMP runs in close collaboration with Materials Management, Quality Control and Quality Assurance.
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Experience in cGMP cell therapy manufacturing. As a member of the Operations and Compliance Support team, you will be part of a team of investigators responsible for the examination and resolution of adverse events (quality events) that occur within manufacturing operations for Client's engineered T-Cell therapy products at the Frederick, Maryland site.
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Cell based bioassays, Flow Cytometry, ELISA and PCR assays. Well versed in various analytical techniques such as Flow Cytometry, ELISAs, PCR, and cell bioassays and other applicable methods to the testing of biopharmaceuticals.
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Key components will be focused on, design and development of innovative qualified and validated immunophenotyping (including high content flow cytometry assays up to 31 markers, receptor occupancy assays, tetramer/dextramer assays as well as immunophenotyping flow based assays), and antigen specific (ELISpot/Fluorospot) or other custom cell based assays.
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General knowledge of the facilities management financial reporting with primary focus on repair and maintenance expenses. High school diploma or general education degree (GED) and a minimum of four years of related experience and/or trade school training.
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AA Degree and 2+ years’ experience in biotechnology or related field and Quality Control experience OR. Job Title - Quality Control Chemist. Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211.
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cell phone jobs Title: general Company: Papa in New Market, MD
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