- Fresenius Medical Center (Tualatin, OR)
- …supports efforts to drive continuous product improvement and cost control. PRINCIPAL DUTIES AND RESPONSIBILITIES: + Supervises all activities related to installation ... Vivonics systems with Fresenius Kidney Care. + Works with ancillary water device manufacturers to assure quality of installations to maintain product reliability,… more
- Stanford University (Stanford, CA)
- …sessions studying the safety and efficacy of investigational medical devices and novel, neurally-controlled assistive interfaces ("brain-computer interfaces") ... in collaboration with finance and/or management staff. + Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study… more
- Teleflex (Morrisville, NC)
- …experience in project or program management working in a technical discipline, medical device and/or engineering preferred. * Proficiency with design control ... :12477 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to...involved with engineering and cross-functional teams in the hardware, software systems space. This position is part of the… more
- Abbott (Santa Clara, CA)
- …potential impact on the business **Preferred** **Qualifications** + Experience in the medical device industry preferred + Experience with clinical trials ... as well as external stake holders including steering committees, and national principal investigators to support device premarket approval (PMA) applications and… more
- Teleflex (Pleasanton, CA)
- …methods and Design of Experiments. * Preferred: 5 years of experience in medical device production or product development. * Preferred: Experience with common ... development to help fuel the Interventional R&D product pipeline. ** Principal Responsibilities** * Plan process development & validation activities...disposable medical device manufacturing processes (eg molding, reflow,… more
- Edwards Lifesciences (Irvine, CA)
- …Solid SAS programming experience on clinical data in the pharmaceutical and/or medical device industry. + 3 years' experience Managing statistical programmers ... regulatory guidelines (eg, GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/ Medical Device research setting + Excellent problem-solving, organizational,… more
- Teleflex (Morrisville, NC)
- …5 years of quality engineering or design assurance experience (preferably in the medical device industry). **Specialized Skills / Other Requirements** * ASQ ... 10% **Requisition ID** :12407 **About Teleflex Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health… more
- Hologic (Newark, DE)
- …a visionary leader with a passion for ensuring the highest standards of quality in medical device design and development? We are seeking a dynamic **Director of ... in FDA Quality System Regulations, especially Design Control requirements, ISO 13485, and Medical Device Directive. + Familiarity with ISO 14970, IEC 60601, IEC… more
- Danaher Corporation (Sunnyvale, CA)
- …possess previous experience in: + Comfortable working in multi-disciplinary environments. + Medical device or regulated industry experience Cepheid, a Danaher ... This role includes the development of firmware and embedded software on ARM architecture within both Linux and real-time...opportunity to: + Onboard under the guidance of a Principal Algorithm Development Engineer to gain expertise in Cepheid's… more
- University of Rochester (Rochester, NY)
- …strategies. May conduct telephone interviews to screen potential study candidates. Reviews medical chart history with Principal Investigator to verify inclusion ... with protocol requirements, such as taking of medications, proper use of device , and/or other interventional activities, to document adverse events and report to… more
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