- AbbVie (Irvine, CA)
- …with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ... our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to...* Prefer at least three years of experience in medical devices , ideally class II devices… more
- AbbVie (Pleasanton, CA)
- …with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ... our talent pipeline and considered for future opportunities. The Device Engineer will work collaboratively with a team to...* Prefer at least three years of experience in medical devices , ideally class II devices… more
- TEKsystems (Dallas, TX)
- …Solutions Consultant to serve as the technical lead for our Clinical Device Management initiatives. This role will be instrumental in designing, developing, and ... lead for the design, configuration, and implementation of ServiceNow Clinical Device Management solutions. * Partner with clinical engineering, biomed, IT, and… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …110 countries and regions. **Summary:** The **Tier 1 Technical Support Specialist (TSS) for Medical Devices in the field of IVD** at the Grifols DxCTS ... **Experience:** Specialist level II: **3 years'** experience with troubleshooting medical devices including technical proficiency an instrumentation or… more
- RWJBarnabas Health (Newark, NJ)
- Director Patient Care Ventricular Assistive Device (VAD) ProgramReq #:0000189067 Category:Professional / Management Status:Full-Time Shift:Day Facility:Newark Beth ... Israel Medical Center Department:Cardiac Recovery Room Pay Range:$125,000.00 - $175,000.00...NJ 07112-2027 Job Title: Director Patient Care Ventricular Assistive Device (VAD) Program Location: Newark Beth Israel Med Ctr… more
- Ricoh Americas Corporation (Indianapolis, IN)
- …in a technical field and 3+ years of experience in manufacturing quality operations medical device industry. + ISO 13485 experience required + Experience working ... such registrar/notified bodies with support from Director level Quality & Regulatory personnel. Job Duties and Responsibilities **Quality System Development and… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- … bodies. + Understanding of regulations, standards and guidelines related to IVD, and/or medical devices and quality systems including 21 CFR, CE-IVD, ISO 13485, ... activities. By working successfully across functions-including Program Management, Marketing, Regulatory , Quality, and Medical Affairs-this leader will ensure… more
- Gilead Sciences, Inc. (Foster City, CA)
- …**Job Description** We are seeking a highly skilled and proactive Senior Device Development Engineer to lead technical development efforts for parenteral drug- ... device combination products, including autoinjectors, prefilled syringes, and needle...+ **Author and review technical reports** and contribute to regulatory submissions (IND, NDA, etc.). + **Collaborate cross-functionally** with… more
- Lilly (Pleasant Prairie, WI)
- …are determined to make life better for people around the world. The Device Assembly and Packaging (DAP) Operations Sr Director is responsible to provide leadership ... Modes Effect Analysis (FMEA). + This role has direct interaction with Regulatory Agencies during site inspections. + Understand and influence the manufacturing… more
- Medtronic (Billerica, MA)
- …and writing in English. **Preferred Qualifications (Must Have!):** + Prior experience in the medical device or electronics industry. + Knowledge of ISO and FDA ... year + 401(k) with up to 6% match + Comprehensive benefits plan, including medical , dental, vision, and more + Fully subsidized Bachelors degree programs paid up… more