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Apply in-depth molecular biology knowledge and experience in the development of CRISPR-based molecular diagnostic assay systems, including development of enzyme reagents and assay workflows.
$105,000 - $135,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Molecular Assay Development team is seeking an accomplished (Senior) Scientist to join our team within the Cellular Therapy Analytical Development (CTAD) organization. The (Senior) Scientist will have extensive hands-on experience in assay development; possess excellent communication skills; and be able to work with cross-functional teams in order to effectively transfer analytical methods, as wells as maintain and troubleshoot existing methods.
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Extensive experience of working with a variety of assay formats and detection technologies such as flow cytometry, high content imaging, ELISA, MSD and HTRF assays. Experience of managing technical aspects of assay development and implementation.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Enthusiastic about playing a pivotal role in the dynamic and multidisciplinary environment of a small biotech, specifically within the realm of microfluidics-based biological assay development.
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Throughout the project, the appointed candidate will utilise a range of skills and techniques including, peptide design and synthesis, assay development and work side by side with biologists to test these in vitro and in vivo.
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Functional characterization (in vitro DNA cleavage) of differential CRISPR-Cas RNP complexes by electrophoretic mobility shift assay (EMSA) or anion exchange (AEX) chromatography. Experience in NGS based assay development and implementation.
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Partners with Clinical Pharmacology PK/PD/ Flow cytometric labs to oversee assay development and review qualification and validation plans, maintenance of SOPs, and identification of critical reagents.
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Prior experience and good understanding of cell-based assay development, cell culture techniques and flow cytometry methods are desired. The Senior Bioanalysis Scientist I is responsible for assay development, validation, and sample testing to support non-clinical and clinical studies for a fast-growing Exelixis pipeline of novel biotherapeutics.
$113,000 - $160,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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The Precision Medicne Pathology group within Precision Medicine supports projects from discovery through CDx assay development. The candidate is expected to design and execute novel tissue-based assay development experiments independently to enhance our biomarker research.
$78Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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This role will engage with customers and colleagues in our commercial and medical organization to provide medical and scientific support for the Oncotype DX assay for breast cancer or the OncoExTra assay for advanced solid tumors, as well as help launch newer products acquired or developed by Exact Sciences.
$175,000 - $263,000Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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We are seeking a highly skilled Bioanalytical Expert to oversee PK, PD, Immunogenicity, and Biomarker assay development, validation, and study phase bioanalysis for our large molecule drug discovery and development programs.
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Prior experience with cell culture and cell-based assay development and T-cell biology. Conducting routine cell culturing and cell-based assay development. Under scientific and technical supervision, the candidate will design and execute cell-based assay advancing multiple discovery programs.
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Demonstrated expertise in GLP and GCP compliance of sample handling and storage, bioanalytical assay development, sample analysis, and laboratory operation and procedures is required. Experience must include a combination of laboratory and project management skills, including managing CROs for assay development and validation for clinical and non-clinical studies.
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Relevant experience consists of working in assay development and/or validation, optimization, experimental design, and data analysis in a regulated industry (cGMP). Ability to independently propose and lead analytical method development projects with purposeful experimental design and the ability to anticipate results that drive towards the conclusions necessary for successful assay development: a successful track record of analytical method development that leads to method validation.
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Demonstrated expertise in GLP and GCP compliance of sample handling and storage, bioanalytical assay development, sample analysis, and laboratory operation and processes is required. Generate and characterize critical reagents to support the assay development and life cycle maintaineces (e.g. Labeling.
$112,000 - $163,000 a yearTemporaryExpandApply NowActive JobUpdated 8 days ago
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