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Our client is seeking a Quality Control Bioassay Consultant to join their dynamic team. Evaluate and approve cGMP analytical data for release and stability testing using bioassay test methods such as mRNA expression, functional potency, and ELISA testing platforms.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Senior QC Analyst will work with others in Quality Control and Analytical Development in a dynamic environment to support AAV-based gene therapy programs. Review and approval of cGMP analytical data for release and stability testing from bioassay test methods including, but not limited to, mRNA expression, functional potency and ELISA testing platforms.
$62 an hourExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Must be trained in GMP Quality systems such as Change Control, CAPA and Deviation; Familiarity with computerized pharmaceutical GMP systems such as LIMS, CDS, BMS, JDE, SAP, Analytical Instrumentation, Manufacturing and Packaging systems, Quality Management Systems, and their associated vendors.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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The ElevateBio ecosystem combines multiple R&D technology platforms – including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform – with BaseCamp®, its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.
ExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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The Quality Control Analyst compiles data for documentation of test procedures that may include stability program testing and formulation studies, participates in the preparation of investigations, summaries and reports, and reviews data obtained for compliance to specifications and reports out-of-trend and/or out-of-specification results.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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We have a current opportunity for a Quality Control Analyst on a contract basis. Author and support quality events; Change Controls, Deviation, CAPA, OOS Investigation, as needed.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Strong attention to detail and a knowledge of cGMP and cGLP regulatory guidelines related to pharmaceutical analytical development and quality control. BS/BA in biochemistry, chemistry, biology, or a related discipline with 3-5 years (Research Associate II) biopharmaceutical industry experience, preferably in gene therapy or other related disciplines.
$85,000 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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The successful candidate must have deep understanding of eQMS software development life cycle (SDLC) in a regulated environment (i.e., cGMP, GCP, GLP) with strong project management and business process analysis skills, and direct experience managing Document Control in a regulated environment.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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The Quality Control Scientist will be responsible for optimization, qualification, transfer, verification, and QC implementation of methods associated with cGMP production of cell and gene therapy drug products and gene editing components.
Full-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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Quality Control and/or Analytical Development experience in Biotech, cGMP areas. We are looking for a Quality Control (QC) professional to join our team as a Senior Analyst Quality Control, supporting our internal GMP cell therapy manufacturing.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Job Title: Quality Control Data Reviewer. Perform cGMP analytical and microbiological data review for various techniques such as HPLC, GC, KF, TOC, Bioburden, endotoxin, TOC, Environmental monitoring, IR and dissolution to ensure adherence to established methodology, procedures and SOPs.
$45 an hourExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Provide technical support for engineering and cGMP manufacturing campaigns (e.g. batch record review, change control management, deviation investigation, etc) in collaboration with other line functions (e.g., Manufacturing Sciences & Technology), as needed.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Previous experience working with quality systems having oversight of cGMP production operations including some or all of the following: batch release, SAP, batch record review. Working knowledge and/or ownership of the following quality systems: Change Control, CAPAs, Deviations, Self-inspection auditing, QA reporting, and approval of GMP documentation.
$60 an hourExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Manager, Quality Control- Cell Therapies provides oversight of a variety of analytical functions that occur in the QC department supporting validation, testing, and reporting of in-process, release, and stability samples.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Research Associate/Associate Scientist will execute Quality Control testing, and associated operations as well as develop analytical assays to support the current and future Vaxess products.
Full-timeExpandApply NowActive JobUpdated 6 days ago
cgmp quality control jobs in Malden, MA
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