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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.
$120,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The individual in this role will perform cGMP QC sample management activities for QC Chemistry, Microbiology, Bioassay, and various Development labs. This position will support first-shift QC Sample Management operations at our client, Wednesday through Saturday.
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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 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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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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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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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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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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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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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.
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Position will participate in production/QC programming, project coordination, CRO management and oversight of vendor programming across Ipsen rare disease studies. Provide statistical programming support to generate derived analysis data sets, tables, listings, and figures for Clinical Study Reports, regulatory submissions, annual IND safety update reports and Integrated summaries (ISS/ISE); create/QC of CDISC SDTM and ADaM files, SAS export files and Define.
$165,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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North American Renewables, Inc., is seeking a Project Manager to join our growing Solar EPC team! Manage assigned larger portions of work and provide clear status reports to primary Senior Project Manager.
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The primary purpose and function of the Practice Manager is to manage the hospital and ensure the highest quality of veterinary care, exceptional client service, associate engagement and maximum productivity of the veterinary medical team.
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In-depth knowledge of human pluripotent stem cell culture, organoids, characterization, QC, and differentiation into neuroectoderm lineage using 2D and 3D cell culture (glia, neuron, and other relevant cell types.
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quality qc manager jobs Title: project manager group in Needham Heights, MA
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