Vice President, Global Regulatory Affairs - Seattle, WA

The Senior Director, Regulatory Affairs, will serve as the Global Regulatory Lead (GRL) and key decision-maker responsible for the development and execution of global regulatory strategy across the company's clinical portfolio.This role offers high autonomy, direct ownership of a ...

The Senior Director, Regulatory Affairs will serve as the Global Regulatory Lead (GRL) and key decision-maker responsible for the development and execution of global regulatory strategy across the company's clinical portfolio. · Global regulatory strategy (Late-Stage preferred) · ...

The Senior Director, Regulatory Affairs, will serve as the Global Regulatory Lead (GRL) and key decision-maker responsible for the development and execution of global regulatory strategy across the company's clinical portfolio. · Global regulatory strategy (Late-Stage preferred) ...

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. · ...

We're hiring a key leader to strengthen our global quality network This role is central to our operations in both the US and Singapore. · ...

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

We are seeking an experienced Quality & Regulatory Affairs Manager to strengthen our global quality network in both the US and Singapore. · Evaluate local operations for continuous compliance with FDA regulations. · Manage inspections and submissions as primary point of contact. ...

The Senior Director, Clinical Regulatory Affairs · reports to the Head of Regulatory Affairs · Independently provide regulatory leadership · Develop registration strategies · ...

The Senior Director Clinical Regulatory Affairs reports to the Head of Regulatory Affairs and is responsible for content development compilation maintenance and review of the Nonclinical and Clinical Modules for regulatory submissions to support Umojas drug products including DMF ...

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 ...

Mozart Therapeutics is an early clinical phase biopharmaceutical company located in Seattle, focused on developing novel immune engagers that specifically target a subset of T lymphocytes to delay the onset and ameliorate pathology of autoimmune diseases. We are developing first- ...

:Mozart Therapeutics is an early clinical phase biopharmaceutical company located in Seattle, focused on developing novel immune engagers that specifically target a subset of T lymphocytes to delay the onset and ameliorate pathology of autoimmune diseases. We are developing first ...

The Director of Regulatory Affairs provides strategic and operational leadership for the regulatory function across ERA Health Research. This role ensures regulatory excellence across all clinical trials while enabling efficient study startups, maintaining continuous inspection r ...

The Director of Regulatory Affairs provides strategic and operational leadership for the regulatory function across ERA Health Research. This role ensures regulatory excellence across all clinical trials while enabling efficient study startups, maintaining continuous inspection r ...

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

The Regulatory and External Affairs Analyst plays a critical role in ensuring the company's compliance with federal and state regulations.As a Regulatory and External Affairs Analyst, this professional is responsible for the collection, · analysis, and submission of data for a va ...

Job Description Summary · Senior Regulatory Affairs professional with 8+ years of experience in medical devices, specializing in US FDA, EU MDR, and APAC regulations. Proven track record in leading 510(k), PMA, and EU Technical Documentation submissions, managing audits and inspe ...

Senior Regulatory Affairs professional with 8+ years of experience in medical devices. · ...

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

Regulatory Affairs Analyst (Open) · Location: Bothell, Washington (Onsite Only · Job Description Summary · Senior Regulatory Affairs professional with 8+ years of experience in medical devices, specializing in US FDA, EU MDR, and APAC regulations. Proven track record in leading 5 ...