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Onto Innovation is a leader in process control, combining global scale with an expanded portfolio of leading-edge technologies that include: 3D metrology spanning the chip from nanometer-scale transistors to micron-level die-interconnects; macro defect inspection of wafers and packages; metal interconnect composition; factory analytics; and lithography for advanced semiconductor packaging.
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We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. Expertise in primary human cell culture, multi-color flow cytometry, multiplex cytokine detection, functional immune cell assays (proliferation, cytotoxicity, chemotaxis) and assay development is essential.
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We’re looking for a Credentialed Veterinary Technician (or a VT currently in the process of completing accreditation) to add their passion, skills, and education to our team. registered vet technician (RVT) veterinary technician (LVT) #veterinary technician specialists (VTS) #certified veterinary technician (CVT.
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The ideal candidate will bring extensive experience in chemical process engineering, with a focus on high-temperature or electrochemical systems and be passionate about sustainability and clean energy production.
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We are looking for a self-directed professional to support Digital Health Technology [DHT] (wearable sensors) and imaging components set-up and monitoring within clinical trials; specifically focused on the operational initiation/set-up, vendor and digital data/imaging monitoring, and data cleaning process efforts that occur within the Biomeasures Endpoints and Study Technologies (BEST) projects.
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You have a degree in a biological science and are capable of quickly coming up to speed on the biologics drug discovery process. This team manages the entire process from partner outreach and engagement, to storytelling and problem solving, to ultimately connecting new partners with the technologies and capabilities they need to solve their problems.
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Utilizing the nursing process, the ECT/TMS/Ketamine nurse is responsible for providing for immediate and long-term nursing care needs of patients receiving ECT/TMS/Ketamine within the standards of the department, hospital and regulatory agencies.
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Providing analytical support to Upstream and Downstream process development team activities by ensuring consistent and timely execution of standardized platform product characterization assays, including data review, storage and trending.
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Provide process and technical leadership in the manufacturing process operations for Drug Substance, including but not limited to: Solution preparation, Adherent and suspension cell culture, Operation of Wave and disposable, single use Bio reactors, Chromatography and Tangential Flow Filtration & Viral Filtration.
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Seurat’s proprietary Area Printing process, developed at Lawrence Livermore National Labs (LLNL), allows metal components to be manufactured at price points and quality levels that compete directly with conventional manufacturing techniques, enabling the reshoring of supply chains and promoting the decarbonization of industry.
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Experience in overseeing or performing critical reagent generation, characterization and qualification for use in Process related impurity assays (Antibodies and conjugated antibodies, enzyme substrates, assay controls, calibration standards etc.
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Plan and oversee the migration of QMS data from TrackWise to Veeva QMS. Ensure data integrity, accuracy, and compliance during the migration process. The ideal candidate will have expert-level knowledge in the architectural design, configuration, and implementation of Veeva QMS systems.
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Gather requirements, convert requirements and design documents into test cases, implement BDD framework, work on datamart projects and data migration process. Must have Master's degree or foreign equivalent in Computer Science, Computer Engineering, Electronic Engineering, or a related field and 2 years experience in the proffered position, or as a Developer, Software Engineer, Technology Analyst, Programmer Analyst, or related occupation.
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Key Information: Owned complete process from design specifications to board assembly/PCB design, prototyping, and vendor collaboration. Responsibilities: Manage complete circuit development process, from specifications to documentation.
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The Engineer will apply cell culture and purification process engineering knowledge in support of technology transfer and clinical/commercial drug substance manufacturing in both stainless and single-use formats.
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process job Title: analyst Company: Kforce in Lexington, MA
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