- Stryker (Flower Mound, TX)
- …May serve as Person Responsible for Regulatory Compliance (PRRC) under the EU Medical Device Regulation + May take responsibility for handling regulatory agency ... of regulatory requirements, including ISO, FDA, and International requirements (ie, Medical Device Regulation) + Demonstrated expertise in regulatory systems… more
- Capgemini (Boston, MA)
- …years of experience in application software development , with 2 years in the medical device or other regulated industries. + Bachelor's or Master's degree in ... clinical outcomes. **Your role** + Design and develop standalone medical device applications using modern C on...related field. + Strong experience with MATLAB for algorithm development and data analysis. + Proficiency in modern C… more
- Baystate Health (Springfield, MA)
- **LVAD** **(Left Ventricular Assist Device )** **Nurse Coordinator- Heart & Vascular** **Full Time** The **LVAD Program Nurse Coordinator- Heart & Vascular** will ... quality, efficiency, and cost-effectiveness of care delivery for Left Ventricular Assist Device . + Collaborate closely with a multidisciplinary team and identified… more
- Fujifilm (Juneau, AK)
- …manager, senior product manager, product/technical director). + Minimum 8 years of medical device experience with strong clinical background. + Prior experience ... global R&D, operations, regulatory, global marketing, infection control, other companies/ device manufacturers, etc.) + Build and maintain strong relationships with… more
- West Pharmaceutical Services (Exton, PA)
- …regulatory/environmental legislations (eg California Prop 65, RoHS, Conflict Minerals, EU Medical Device Regulation) for all West global product portfolios ... Bachelor's with 5+ years required; or + Master's degree/PhD 2+ years medical device regulatory experience required **Preferred Knowledge, Skills and Abilities**… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …field required; _Master's degree preferred_ + Expert-level proficiency in ISO 13485, Medical Device Regulation (MDR), and FDA requirements with demonstrated ... ISO frameworks, GMP/GDP protocols, and USP-EP guidelines as they apply to medical device environments + Demonstrated capability to align technical decisions… more
- Southern California Institute of Technology (Anaheim, CA)
- …students enrolled in the biomedical technology programs on topics related to medical device operation, maintenance, repair and other topics related to ... Responsibilities + Deliver comprehensive instruction on subjects such as medical equipment technology, device installation and operation, engineering… more
- Hologic (Marlborough, MA)
- …7+ years of product management and/or marketing experience in the medical device , diagnostics, or laboratory environment. + **Education:** Bachelor's ... An MBA is preferred + **Digital & IT Expertise:** Knowledge of digital pathology, medical device software, or IT integration within a clinical or laboratory… more
- Zimmer Biomet (Fort Worth, TX)
- …skills. * Influence the direction of key decision makers and influencers. * Knowledge of medical device business and medical device market. * Knowledge ... innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's...world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible… more
- GE HealthCare (Bellevue, WA)
- …of the digital manufacturing strategy, product data mastering, design transfer, Device Master Record and International Trade Compliance Submission. GE HealthCare is ... a leading global medical technology and digital solutions innovator. Our mission is...the teams and drive program execution. + Own product Device Master Record(s) and creation of necessary product artifacts… more