Draper Laboratories jobs

Scientist, Analytical Development and Quality Control Brisbane, CA Company Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Position Nurix Therapeutics seeks an experienced Scientist to join the Analytical Development and Quality Control group. The Scientist will conduct analytical method development and material characterization studies to inform drug substance and drug product development. They will also provide operational oversight at external CDMO/CTL partners, manage reference standards and impurity markers, collaborate in CMC risk management, and author technical reports. In Nurix's laboratories, the Scientist will characterize material attributes and impurities by high resolution mass spectrometric and multidimensional chromatographic techniques. They will determine impurity structures, characterize material stability, and elucidate mechanisms of degradation. They will employ state of the art QbD approaches to develop and troubleshoot chromatographic test methods to accelerate and derisk QC activities performed externally at CDMOs and CTLs. The Scientist will critically evaluate characterization data and communicate results in multidisciplinary teams. The ideal candidate must have demonstrated expertise

Digital Engineering Data Solutions Architect (MTS2) 2 Locations posted: Posted 30+ Days Ago

Senior Financial Analyst Cambridge, MA posted: Posted 7 Days Ago

Flight Compute Software-in-the-Loop Simulation Engineer Cambridge, MA posted: Posted 30+ Days Ago

Cyber Effects Group Lead Cambridge, MA posted: Posted 30+ Days Ago

Special Security Programs Manager Cambridge, MA posted: Posted 7 Days Ago

Senior Navigation Algorithm Engineer Cambridge, MA posted: Posted 8 Days Ago

Principal Embedded Software Engineer Cambridge, MA posted: Posted 17 Days Ago

Electro-Mechanical Instrument Co-op Cambridge, MA posted: Posted 30+ Days Ago

Incoming Quality Control (IQC) Inspector III – Mechanical Middle River, MD ABOUT ROCKET LAB Rocket Lab is an end-to-end space company delivering responsive launch services, complete spacecraft design and manufacturing, payloads, satellite components, and more - all with the goal of opening access to space. The rockets and satellites we build and launch enable some of the most ambitious and vital space missions globally, supporting scientific exploration, Earth observation and missions to combat climate change, national security, and exciting new technology demonstrations. Our Electron rocket has become the second most frequently launched U.S. rocket annually and has delivered more than 230 satellites to orbit, all while we work to develop Neutron, our upcoming medium-lift, reusable launch vehicle for larger constellation deployment. Our Space Systems business designs and builds our extensive line of satellites, payloads, and their components, including spacecraft that have been selected to support NASA missions to the Moon and Mars and components used on the James Webb Space Telescope. NEUTRON Neutron is a medium lift launch vehicle capable of delivering the mega constellations of tomorrow, high assurance payloads, and human spaceflight. As a highly reusable launch platform, Neutron will deliver a highly cost-effective and reliable launch solution leveraging Rocket Lab's proven execution history with the Electron program. If you're interested in joining a high performing team, pushing the boundaries with a clean sheet development of re-usable liquid launch vehicle, this is your opportunity! I NCOMING QUALITY CONTROL (IQC) III - MECHANICAL As a Incoming Quality Control (IQC) Inspector

Principal Digital Electronics Engineer Clearfield, UT posted: Posted 9 Days Ago

Senior Software Autonomy Engineer Cambridge, MA posted: Posted 30+ Days Ago

Software Guidance Navigation & Control Engineer for Space Applications Houston, TX posted: Posted 10 Days Ago

Principal RF Communications Engineer Cambridge, MA posted: Posted 11 Days Ago

Group Leader, Electro-Optics Integration Cambridge, MA posted: Posted 10 Days Ago

Principal Power Electronics Engineer Cambridge, MA posted: Posted 11 Days Ago

Senior Director, Commercial Manufacturing, Science and Technology Remote, United States Who We Are: Cogent Biosciences is a publicly traded biotechnology company focused on developing novel precision therapies to treat a broad range of patients with unmet medical needs. Cogent's lead program, bezuclastinib, is designed to selectively and potently inhibit exon 17 mutations found within the KIT receptor tyrosine kinase, including KIT D816V. KIT D816V is responsible for driving a rare and serious condition called Systemic Mastocytosis, and exon 17 mutations are also found in patients with gastrointestinal stromal tumors (GIST), a type of cancer with strong dependence on oncogenic KIT signaling. Bezuclastinib has exhibited promising initial data across all three trials: APEX in AdvSM, SUMMIT in NonAdvSM and PEAK in GIST, including an encouraging safety profile across 600+ patients in single agent and combination dosing. The Role: This position oversees late phase through commercialization small molecule drug product manufacturing at partner Contract Development and Manufacturing Organizations (CDMOs) and ensures high-quality products are delivered on time and within budget. Serve as a technical expert who leads the transfer of manufacturing processes to commercial scale. Manage processes, systems and infrastructure that meet safety, cGMP manufacturing, and regulatory compliance. Provide technical expertise and oversight for process validation, lifecycle management, and continuous improvement. Anticipate and solve complex manufacturing issues. Work in collaboration with internal and external stakeholders including CMC, Quality, Supply Chain and Regulatory, as well as CDMOs. Responsibilities: - Lead commercial drug product CMC lifecycle activities such as post-approval change management, process validation

Space and Strategic Navigation Engineer Cambridge, MA posted: Posted 8 Days Ago

Principal Radiation Effects Engineer Huntsville, AL posted: Posted 30+ Days Ago

Flight Software Engineer, Distinguished Cambridge, MA posted: Posted 30+ Days Ago

Senior Analog Mixed Signal ASIC Layout Engineer Cambridge, MA posted: Posted 11 Days Ago

Principal Acoustic Systems Engineer Cambridge, MA posted: Posted 11 Days Ago

Mixed-Signal Electronic Design Engineer 2 Cambridge, MA posted: Posted 3 Days Ago

Program Manager 2 - Sensor Development Cambridge, MA posted: Posted Yesterday