Clinical Affairs Specialist - Bothell

As a temporary Clinical Affairs Specialist, you will use your strong prior planning, communication, and coordination skills to assist in the design, development and testing of Fujifilm Sonosite's point-of-care ultrasound systems. · ...

This role is part of the global design and development teams supporting the Philips Oral Healthcare business unit, · which delivers power toothbrushes, power flossers and whitening solutions to millions of customers worldwide.This Regulatory Affairs Specialist will assist with im ...

As a Clinical Affairs Specialist at Fujifilm Sonosite, you will use your strong planning skills to assist in designing ultrasound systems. · ...

+ Develops and facilitates regulatory submissions for new products/solutions. · + Identifies potential regulatory approval risks based on changes in regulations... · + You're The Right Fit If you have a Bachelor's or Master's degree in Chemistry... ...

· Position Overview · As a temporary Clinical Affairs Specialist, you will use your strong prior planning, communication, and coordination skills to assist in the design, development, and testing of Fujifilm Sonosite's point-of-care ultrasound systems. Your attention to detail a ...

This is a temporary Clinical Affairs Specialist role at Fujifilm Sonosite where you will assist in the design and development of point-of-care ultrasound systems. · ...

We reinvent how healthcare is delivered with point-of-care ultrasound technology. As a temporary Clinical Affairs Specialist, you will use your strong prior planning, communication, and coordination skills to assist in the design, development, · & testing of Fujifilm Sonosite's p ...

+ Clinical Affairs Specialist: As a Clinical Affairs Specialist, you will use your strong prior planning, communication, and coordination skills to assist in the design, development, and testing of Fujifilm Sonosite's point-of-care ultrasound systems. · 3-5 years of complex proje ...

+Responsibilities:This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe... · Requirements: · B.S. degree or higher in a life science or technical discipline... · ...

We are seeking an experienced medical devices regulatory affairs professional to develop and execute regulatory strategies and manage product submissions for novel hardware and software as a medical device (SaMD) products for distribution into worldwide markets. · Act as the core ...

The Supervisory Public Affairs Specialist is based at the VA Puget Sound Healthcare System. · Serve as facility spokesperson - strategic consultant and media advisor to leadership - service line leaders - and program managers · Responsible for work assignments - leave approval - ...

This position is responsible for regulatory submissions required to market medical devices in both the U.S. and Europe. · Prepare regulatory submissions required to market medical devices in both the U.S. and Europe. · Support international product registrations. · ...

This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe. · ...

Description · How do you get items to customers quickly, cost-effectively, and—most importantly—safely, in less than an hour? And how do you do it in a way that can scale? Our teams of hundreds of scientists, engineers, aerospace professionals, and futurists have been working har ...

We are delivering to customers and are excited for what's to come. · The Opportunity · As Amazon Prime Air expands its drone delivery service,This is a pivotal role in which you will shape the regulatory landscape for commercial drone delivery,You will serve as a bridge between A ...

We are delivering to customers and are excited for what's to come. If you are seeking an iterative environment where you can drive innovation, apply state-of-the-art technologies to solve real world delivery challenges, and provide benefits to customers, Prime Air is the place fo ...

We are seeking a Manager of Regulatory Affairs to drive regulatory strategy and execution for our medical device portfolio... · ...

The Regulatory Specialist will support end-to-end CFG and export certification activities for global markets. · CFG & Export Certificate ManagementPrepare submissions via CECATS for product familiesClean up outdated product codesU.S. Marketing Status Verification · ...

We are seeking a Director U.S. Market Development to lead commercial market development activities in preparation for the potential launch of varegacestat in desmoid tumors. · ...

Operations Specialist Job summary: Job Description · This position plays a key role in supporting EMSA departments with navigating complex university systems, · oversees the Operations Team's Liaison Program, · supports campus wide initiatives, procurement,and special projects. · ...