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Keywords: Go, Golang, Python, AWS, Kafka, Spark, SQL, Hybrid remote, Massachusetts, Senior Software Developer, Go Software Developer, New development, Greenfield. Vestmark is actively looking for a motivated Senior Software Engineer with Go and Python development experience and large-scale data streaming and processing experience.
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Align early assay development procedures and ensure appropriate validation/verification documentation for new releases and changes to the product. The CLIA Quality Manager will collaborate with direct and/or delegated authority to ensure the CLIA Quality Management Systems (QMS) are effective and compliant with applicable requirements, provide leadership and guidance re: CLIA and associated regulations, and support the Lab Director and leadership in maintaining audit readiness.
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PHD candidates in Engineering/ IT/Computer Engineering/Computer Science/Bioinformatics or related discipline with relevant with a minimum of 3 years of experience in software development and pipeline automation in the pharmaceutical and/or biotech industry.
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A bachelor’s degree in Engineering/ IT/Computer Engineering/Computer Science/Bioinformatics or related discipline with a minimum of 7 years of experience in software development and pipeline automation in the pharmaceutical and/or biotech industry.
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This individual will be responsible for designing, developing, and implementing fit-for-purpose methods across various technologies, such as ELISA, MSD, Luminex, ELLA, Quanterix, to support early through late-stage drug development programs to inform on target engagement, pharmacodynamics, pharmacokinetics, mechanism of action, and safety, to advance RNAi therapeutic development.
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PHD candidates in Engineering/ IT/Computer Engineering/Computer Science/Bioinformatics or related discipline with relevant with a minimum of 1 years of experience in software development and pipeline automation in the pharmaceutical and/or biotech industry.
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Experience in analytical method development, especially understanding in molecular assays for T cell product characterization and release. Perform molecular assay development involving qPCR, ddPCR, associated primer and probe design for the characterization of genetically engineered primary T cells.
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Reporting to the Associate University Archivist for Collection Development and Records Management Services (AUACDRMS), the SRMA will provide leadership in the development and implementation of a model and comprehensive University records management program that both protects the interests of the University and also contributes to its educational and research missions by providing records stewardship guidance to Harvard staff.
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Ph. D. in Biochemistry, Molecular Biology, Bioengineering, or related field with a demonstrated record of productivity
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Support DMPK project representatives in coordinating discovery and development PK and PK/PD studies. Research Associate- DMPK preclinical study coordinator. We are seeking a highly motivated and well organized scientist to join the Drug Metabolism and Pharmacokinetics (DMPK) department.
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Strong background in mammalian cell culture, stable cell line generation, and process development. Expertise and hands-on experience with protein purification methods used in discovery and process development.
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The Research Engineer will be focused on iterative device development, ingestible/implantable electronics, embedded software development, machine learning integration, and novel drug delivery/bio-sensing system design for treatment of a variety of disease conditions.
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The Machine Design Engineer will be a member of the Advanced Manufacturing Team focused on developing the next generation high volume manufacturing processes that will connect 24M’s revolutionary product to the high growth energy storage market.
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Negotiates cross-functionally, successfully motivates and influences (Clinical Development, Regulatory Affairs, CMC, QA, Pharmacovigilance, etc.) In conjunction with the CRO, identifies required study specific training of the clinical staff, ensuring understanding of the drug development process and knowledge of international standards (GCP/ICH), the requirements and compliance with the appropriate health authorities (FDA/EMEA), and the application of the aforementioned to the entire study.
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Associate Director, Downstream Process Development (Proteins) 2033669. Strong relevant industry experience in downstream process development for proteins. PhD or Masters with extensive background leading a team engaged in protein biologics process development.
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product development jobs Title: line cook in Cambridge, AK, West Virginia
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