- Edwards Lifesciences (Irvine, CA)
- …+ Bachelor's Degree in related field, 12+ years of relevant experience in medical device marketing or healthcare industry required OR + Master's Degree ... Medical Affairs on the APTURE publication strategy + Support Therapy Awareness and Market Development initiatives + Regularly...in related field, 10+ years of relevant experience in medical device marketing or healthcare industry **What… more
- West Pharmaceutical Services (Exton, PA)
- …legislations (eg California Prop 65, RoHS, Conflict Minerals, EU Medical Device Regulation) for all West global product portfolios + With minimal ... Bachelor's with 5+ years required; or + Master's degree/PhD 2+ years medical device regulatory experience required **Preferred Knowledge, Skills and Abilities**… more
- Zimmer Biomet (Warsaw, IN)
- …segment by focusing on the four P's + Competitive and financial analysis + Update product information literature + Support medical and sales education events ... of belonging. **What You Can Expect** Responsible for providing support to the Global Revision Knee product ...and influence others through detailed knowledge of orthopedic and medical device industry + Microsoft Office Suite.-… more
- Abbott (Sylmar, CA)
- …diverse and growing portfolio of digital health products, including software as a medical device (SaMD), connected devices, and digital health platforms. This ... Solutions leadership and portfolio program teams to prioritize AI investments that support Abbott Medical Devices' strategic direction; Assist in assessing and… more
- J&J Family of Companies (Raynham, MA)
- …general direction and can exhibit an attention to detail. + Interested in medical device /orthopaedic fields. + Able to establish and cultivate collaborations and ... competent, with experience in computer-aided design and drafting, mechanical testing, and medical device documentation highly desirable. + Previous internship in… more
- Abbott (Alameda, CA)
- …as they relate to the development, verification, validation, and maintenance of application in support of medical device software. + Software Quality lead in ... to the development, verification, validation, use, and maintenance of medical device software. + Coordinate activities with...of those reviews and delivery on schedule. + Considered Non- Product SWQA compliance SME in support of… more
- Caldera Medical (Westlake Village, CA)
- …your role as a Sr. Regulatory specialist, you will develop and implement medical device regulatory strategies to obtain timely approvals from worldwide ... provide regulatory input and guidance to cross-functional partners regulatory documentation for medical device approvals in compliance with EU MDR, MDSAP, NMPA,… more
- Amazon (Seattle, WA)
- …You will work in a highly collaborative environment, partnering with other Devices product lines and internationally to share best practices and coordinate on new ... hypothesis for how to help customers discover the right product . You will conceive and propose new strategies and...channel performance. Your goals will be to maximize incremental device sales and improve customer experience. You will test,… more
- Abbott (Santa Clara, CA)
- … management/marketing experience required (or master's degree/MBA with 4+ years' experience). * Product management experience in medical device and/or pharma ... * Partner with Key Opinion Leaders to gather insights and advocate for product adoption. * Support international congresses and symposia with messaging,… more
- Medtronic (Northridge, CA)
- …teams to ensure compliance with ISO 10993 standards and global medical device regulations. The role also supports product development by designing and ... clear, concise, and well-structured test plans and reports to support regulatory submissions. This role involves coordinating required chemical characterization… more