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Define, and apply the manufacturing quality toolset including NCR, SCAR, SRB, MRB, PFMEA, IQ, OQ, PQ, GR&R/measurement system analysis, control plans, process verification/validation plans, validation protocol development, Cpk/PpK, Cp, SPC, incoming inspection plans, inspection methods, DOE, process data analysis, and DMAIC/PSP.
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Experience with leadership communications, risk communications, and incident response team (IRT) protocol. Investigate, research and deeply understand both current trends and future forecasts in integrated marketing, brand marketing, experiential marketing, strategic communications and digital communications which may contribute to the continual improvement of the Compass at Google program marketing and communications strategy.
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The Mammography Technologist performs high quality mammography procedures, according to exam protocol, in a timely manner. Focus Staff is seeking a traveling Certified Mammography Tech, who will perform mammography procedures on ambulatory and hospital patients in a physician office, clinic, or hospital setting as requested by a physician or other licensed provider for the diagnosis of disease and injury in accordance with established protocols.
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Reporting to the Breast CRG Clinical Research Manger, the Clinical Research Coordinator Associate - Breast Oncology will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to ensure protocol requirements are carried out and data quality is maintained.
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This position regularly leads marketing and communications activations in support of broader Food program objectives across workstreams including nutrition and behavioral science, sustainability, risk management, culinary, people operations, DEI and digital innovation.
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Our CLS work exclusively in Transfusion Services where they rotate through several benches: maintain competency in lab technician skills (receiving blood products/reagents, test product request accessioning, blood product modification, issue, and return), patient specimen testing on automated platform and manual serological methods, Charge Tech handling of emergency release protocol, and Immunohematology Reference Lab (IRL) with advanced antibody workups.
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Experience in cellular protocol stack (e.g., NAS/RRC/PDCP/RLC/MAC/PHY/SDAP), control/data plane. Experience in cellular protocol and technical leadership. Experience with wireless technologies (e.g., 5G NR, LTE-FDD/LTE-TDD, NB-IOT, NTN, DSDS.
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Experience in all aspects of protocol conduct, both early and late phases, including protocol writing, start-up, study execution, analysis, and reporting Sufficient content expertise to be able to meaningfully contribute to document development and data review and interpretation under the direction and oversight of the CMO. Knowledge of applicable FDA Code of Federal Regulations, Good Clinical Practices, and clinical trials guidelines is required.
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Expertise in seat belt routing, dummy positioning , seat squash and mechanism adjustments using state of art CAE as necessary to suit protocol and test setup requirements. Advanced user of tools such as: Ansa, LS-Dyna, Meta-post, Primer, Hyperworks etc.
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Deep understanding of 4G and 5G; 3GPP specifications with focus on Physical and MAC layers, Understanding of protocol stack procedures with knowledge on RRC, RLC, PDCP and NAS layer is plus. Verify key protocol, signal processing and numerical algorithms with very tight time, latency and energy budgets.
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Partner with scientists to improve analytical methods for QC of molecular biology protocol steps. BA or MS biology or a related field with 1+ years of laboratory experience. Extensive hands-on experience with PCR and troubleshooting molecular biology workflows.
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Supports end -to-end clinical supply responsibilities including but not limited to protocol interpretation, demand planning, supply planning, distribution, inventory management, label generation and planning and execution of labeling operations at partner contract manufacturing organizations (CMOs.
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You should be comfortable with microcontroller peripheral control buses such as SPI, UART, I2C, JTAG, etc., with at least some basic knowledge of device drivers, boot loaders, and communication protocol stacks.
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You will work collaboratively within cross-functional teams (eg, Regulatory Affairs, Clinical Research, Clinical Operations, Clinical Pharmacology, Global Patient Safety, and Clinical Data Science) to lead protocol development for large clinical programs and drive document strategy for Medical Writing.
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The Senior Supplier Quality Engineer is responsible for quality engineering and management activities with suppliers driving quality improvement, ensuring compliance, and supporting Value Add Value Engineering (VAVE) / Expansion project activities.
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protocol job in Menlo Park, CA
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