- Stryker (San Jose, CA)
- …** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SiMD) or Software in a Medical Device (SiMD) ... strong technical skills + Experience with regulatory agencies (FDA, MoH, TUV) and medical device regulations (820, IEC 62304/82304, 60601), with experience in… more
- DEKA Research & Development (Manchester, NH)
- …a Product Complaints Engineer - Team Lead to work in a dynamic Medical Device Research and Development environment. The position reports to the Product ... / other regulatory requirements. + Identify and make sound decisions regarding medical device reporting to regulatory agencies. + Interface with Third… more
- Integra LifeSciences (Plainsboro, NJ)
- …policies, US Food and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical Device Regulations ... set new standards of care. The **Sr. Q** **uality Engineer / Quality Operations (Validations, Risk Management & Statistics)**...Drug Administration (FDA) regulations, ISO 9001, ISO 13485:2003, Medical Device Directive (MOD), the Canadian … more
- Lilly (Indianapolis, IN)
- …A minimum of 2 years of work experience in GMP regulated pharmaceutical and/or medical device industries is required. + Background in sterile barrier and/or deep ... Eli Lilly and Company supports the design, development, and commercialization of drug products and pharmaceutical delivery systems including medical devices and… more
- ManpowerGroup (Savannah, GA)
- Our client, a leading organization in the medical device manufacturing industry, is seeking a dedicated and experienced Quality Engineer to join their team. ... 7-10 years of experience in quality engineering within the medical device industry. + Significant experience with...completion of waiting period consultants are eligible for:** + Medical and Prescription Drug Plans + Dental… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- …methods is required. Familiarity with Design Control requirements and knowledge of Medical Device Validations is preferred. **Education and Experience:** + ... **Job Description Summary** The Quality Engineer II is responsible for the application and...Control, or Product/Process non-conformance investigations + Experience in a medical device or pharmaceutical manufacturing facility. +… more
- Veterans Affairs, Veterans Health Administration (White River Junction, VT)
- … equipment and/or technology. Manages a recall and safety alert program for medical devices, including medical device incident investigations to assure ... Summary The Supervisory Biomedical Engineer (Clinical) position is in the Clinical Engineering... (clinical) is responsible for compliance and reporting of medical device cyber security and isolation for… more
- Teleflex (Plymouth, MN)
- …The Senior R&D Engineer is responsible for, managing quick turn medical device OEM projects, responding to Requests for Quotes, and prototyping ... global provider of product development and production services for medical device manufacturers. We set ourselves apart...for this position will also include benefits such as medical , prescription drug , dental and vision insurance,… more
- Fresenius Medical Center (Lexington, MA)
- …troubleshooting skills. + Excellent written and verbal communication skills **Fresenius Medical Care maintains a drug -free workplace in accordance with** ... and existing systems on multiple platforms. **IT - WINDOWS ENGINEER FOCUS:** + Proven ability to write PowerShell, VBScript....Directory and Azure Active directory + Understanding of mobile device management for iOS and Android + Knowledge of… more
- Sandia National Laboratories (Albuquerque, NM)
- …Requirements for MedPEDs: If you have a Medical Portable Electronic Device (MedPED), such as a pacemaker, defibrillator, drug -releasing pump, hearing aids, ... of onsite work and working from home) + Generous vacation, strong medical and other benefits, competitive 401k, learning opportunities, relocation assistance and… more