Senior Director Regulatory Affairs - Seattle

The Company is seeking a Head of Regulatory Affairs to provide strategic leadership and oversight of all regulatory activities related to the development and registration of its products. · The successful candidate will be responsible for providing regulatory strategic input to n ...

Support and advise cross-functional teams and communicate APAC regulatory requirements and challenges effectively to meet project needs and company objectives. · ...

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) ...

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. · ...

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. ...

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. · ...

The Company is seeking a Vice President for Regulatory Affairs in Oncology. The successful candidate will be a strategic thought partner, deeply experienced in oncology, with a focus on leading the development of all non-clinical and clinical regulatory strategies. · This include ...

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 ...

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 ...

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

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 ...

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

The Regulatory and External Affairs Analyst plays a critical role in ensuring the company's compliance with federal and state regulations. · Prepare, review, and submit reports to federal and state agencies by compiling and analyzing financial and operational data, ensuring accur ...

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

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 ...

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 ...