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The QA/QC Manager, a pivotal role in our organization, will be responsible for quality control, quality assurance, quality management, and Good Manufacturing Practice (GMP.
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Our client seeking a contract role in Quality Control Sample Management Associate II based at their Norwood, MA site. General knowledge of industry standards and guidelines for quality control laboratory operation.
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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.
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The Scientist, Analytical Development & Quality Control is responsible for analytical development, feasibility, method qualification, routine, and stability testing of antibody drug conjugates and intermediates.
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Execute QC molecular biology and Bioassay methods (e.g. qPCR, sequencing, protein expression (cell based and cell free) In this role, you will support cGMP QC testing for raw materials, drug substances, and finished products at the company's manufacturing facility and affiliated contract organizations.
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You will implement quality control (QC) protocols to define key attributes and processing parameters for Tender's plant-based meat products. You'll get to work with a diverse group of people that care deeply about what we are trying to solve.
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Experience as a radiation oncology medical physicist, including clinical experience with linac calibrations and QC, treatment planning system QC and routine use, sealed isotope therapy and radiation safety, IMRT planning and delivery, computer systems quality control, and medical physics program documentation.
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Develop computational pipelines (e.g., with Nextflow, Snakemake, or WDL) for a variety of Research and Development applications, with particular focus on in vitro and in vivo mRNA screening assays; next-generation sequencing (NGS) data and analysis; and the design, assembly, and quality control (QC) of pDNA and mRNA vaccines and therapeutics.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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The QC Associate will support GMP testing in QC laboratories at our BaseCamp facility in Waltham. Work cross-functionally with Analytical Development and other QC functions to assist in the qualification of developed assays.
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Manage and develop the team responsible for the Quality Control Raw Materials program, the QC Raw Materials Testing Laboratory and outsourced raw material testing labs. BS in a scientific discipline with 8 years’ experience in pharmaceutical / biotech industry within Quality Control or Quality Assurance, at least 4 years managing QC Testing Laboratory.
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Knowledge of how to implement QC requirements with a variety of downstream in-vitro and in-vivo uses. Understanding the importance of how to develop production workflows and appropriate QC for in-vivo grade products is essential to the role as downstream uses include immunogenicity assays, in-vivo PK, efficacy and toxicology studies.
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Validate antibody performance by WB, IHC, ICC, FC, and IP at QC stage for Reagent projects. The successful candidate will be responsible for RabMAb development by performing experiments of antibody screening, and validation using sELISA, WB, IHC, ICC, FC, IP techniques to ensure high quality RabMabs to be developed for life sciences, across all delivery destinations (Catalogue, partner, custom, and collaborator.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Your job, as Quality Control Data Reviewer - QC Chemistry within our Quality team, will be to provide quality support and guidance of assays to Quality Control Chemistry for release of life-saving products to our patients.
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The role will support the GMP-validation of assay-automation in a fast-paced Quality Control laboratory located in Cambridge, Massachusetts. We are seeking an Sr. Specialist, QC Automation, to support the transition of GMP release and stability assays onto automated platforms for cell and gene therapy products.
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At least 10 (BS), 8 (MS), 0 (PhD) years’ experience in analytical development or quality control, mostly supporting antibody or ADC therapeutics under GMP. Technical and GMP expert that will be responsible for leading analytical method lifecycle activities at external AD/QC laboratories for late-phase antibody-drug conjugate (ADC) development.
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quality control qc jobs Title: project manager group in Needham Heights, MA
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