Vice President/Executive Director, Medical Affairs - Bothell

The Vice President/Executive Director, Medical Affairs will lead three key functions—Medical Science Liaisons (MSLs), Patient Advocacy, and Medical Information. · ...

+ Ensure product compliance with applicable global environmental and chemical regulations Collaborate with Regulatory Affairs and Quality to ensure alignment with ISO 13485 Strong documentation regulatory interpretation and cross-functional collaboration skills + Bachelors degree ...

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 ...

Senior Regulatory Affairs professional with 8+ years of experience in medical devices, specializing in US FDA, EU MDR, and APAC regulations. · ...

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. · We are all in it together to make a difference.Be a part of a culture that doesn't just wait for change but actively creates it—whe ...

+Job summary · Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. · +ResponsibilitiesDefine and lead the global medical strategy for Soltas aesthetics device portfolio. · Serve as the ...

+Job Summary:Today Pfizer Oncology has an industry-leading portfolio of 25 approved innovative cancer medicines. · ++Support the development maintenance and oversight of medical project plans. · Manage project schedules timelines budgets and plans for project quality resources an ...

Sr. Manager Oncology Scientific Communications is responsible for operational execution of key logistical tasks for major medical congresses. · Support medical congress strategy · Manage approved vendors · Gather insights to enable knowledge sharing · ...

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 ...

The Global Strategic Marketing (GSM) and Services Marketing Coordinator will assist in developing initiatives such as global user advisory boards voice of customer activities cross-functional meetings project management planning duties administrative operational support. · Organi ...

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—wher ...

The Medical Safety Manager independently oversees safety surveillance activities for medical products by analyzing data from post-marketing surveillance, · literature reviews, · and real-world evidence to identify risks and ensure patient well-being. ...

We're looking for a Clinical Affairs Specialist to assist in the design, development, and testing of our point-of-care ultrasound systems. · ...

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. · ...

+ 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... ...

Puget Sound Energy is looking to grow our community with top talented individuals like you. · Is responsible for daily/shift operations and work-flow to meet established service and quality levels, · including accuracy, productivity, budget and targets.Resolves customer issues · ...

The Localization Project Manager III is responsible for planning, executing, and continuously improving translation and localization projects for Verathon medical device products. · Plan, scope, schedule, and manage medium-to-large translation and localization projects. · Serve a ...

The Clinical Development Scientist will manage the direction and evidence collection of Philips Oral Healthcare products.The role involves designing clinical trial protocols and studies, preparing reports and regulatory submission documents using advanced software skills while ma ...

The LIMS Application and Instrument Support Specialist will provide on-site support for a STARLIMS implementation at the Food and Drug Administration (FDA) Office of Regulatory Affairs (ORA). · Application Support ExperienceLIMS and/or ELN Experience Preferably STARLIMSLab Instru ...

The Localization Project Manager III is responsible for planning, executing and continuously improving translation and localization projects for Verathon medical device products and related content. · • Plan, scope, schedule and manage medium-to-large translation and localization ...