- Global Foundries (Essex Junction, VT)
- …GlobalFoundries is a leading full-service semiconductor foundry providing a unique combination of design, development, and fabrication services to some of the ... etc). + Define and optimize III-V superlattices, buffers, and device layers and requirements as defined in the Technology...upon the successful completion of a background check and drug screen, as applicable and subject to applicable laws… more
- Abbott (Plymouth, MN)
- …surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements world-wide are current, up-to-date ... are new or modified, are distributed to appropriate personnel. + Reviews device labeling and marketing materials for compliance with FDA submissions and applicable… more
- University of Pennsylvania (Philadelphia, PA)
- …start-up, creating consents, IRB submissions, recruitment, enrollment, AE management, investigational drug and device management, data entry, resolution of ... activities including recruitment, management of study materials, IRB submissions, device and supply management, and biosample handling (collection, shipping and… more
- Abbott (St. Paul, MN)
- …to perform regulatory activities for a transcatheter heart valve replacement device . **The Opportunity** As an individual contributor, this position performs ... + Creates, reviews and approves engineering changes. + Reviews and provides input on device labeling. + Acts as core team member providing review and analysis of… more
- DISH Network (Littleton, CO)
- …for Apple and Boost Mobile retail channels; focus on optimizing device go-to-market processes, overcoming launch-gating bottlenecks, and ensuring quality, on-time ... Apple adoption and market success at Boost Mobile by crafting compelling device positioning, executing targeted device go-to-market tactics, and equipping sales… more
- Takeda Pharmaceuticals (Boston, MA)
- …and their amendments/supplements). + Understanding of scientific principles and regulatory Device requirements relevant to global drug development and ... is inclusive of 6 years of regulatory experience or combination of 8 years regulatory and/or related experience. +...experience includes reviewing, authoring, or managing components of both drug and device regulatory submissions. + Understands… more
- University of Pennsylvania (Philadelphia, PA)
- …subjects and the family of potential participates in the trial which includes the device / drug , procedure and follow up to ensure informed consent is obtained. ... and 1 to 2 years of experience or equivalent combination of education and experience is required. CRC B:...of potential participates in the trial which includes the device / drug , procedure and follow up to ensure… more
- Lilly (Indianapolis, IN)
- …by advancing patient safety, usability, and effectiveness across medical devices and drug -led combination products? The DDCS Human Factors Team proactively ... / Principal Engineer with an advanced understanding of pharmaceutical and/or delivery device development with the learning agility and ability to apply Human Factors… more
- Veterans Affairs, Veterans Health Administration (Portland, OR)
- …following: Will provide sterilization, preparation, supply items and reusable medical device decontamination and distribution support for the medical center. The ... care including instrumentation (scissors, forceps, retractors, etc.), reusable medical device (suction machines infusion pumps, etc.), surgical trays and sets… more
- Veterans Affairs, Veterans Health Administration (Pittsburgh, PA)
- …responsible for the receipt of contaminated critical and semi-critical reusable medical device (RMD) and for the decontamination and sterilization of this RME. The ... for the occupation. Receives contaminated critical and semi-critical reusable medical device (RMD) in the decontamination area, and may receive noncritical equipment… more