Director, Regulatory Affairs - Redmond, WA

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. · ...

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 ...

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. · ...

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 ...

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

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 ...

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 ...

+ 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... ...

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 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 ...

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 ...

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 · ...

Microsoft is looking for a skilled attorney to join our Corporate, External, and Legal Affairs (CELA) team as the Principal Corporate Counsel for Privacy Advocacy and Regulatory Affairs (PARA). · ...

Microsoft is looking for a skilled attorney to join our Corporate External and Legal Affairs (CELA) team as the Principal Corporate Counsel for Privacy Advocacy and Regulatory Affairs PARA. · Contribute as a member of the team responsible for guidance on data protection and priva ...

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.This role offers high autonomy, direct ownership of a ...

We are seeking a Regulatory Affairs Specialist (Contractor) with hands-on experience in China NMPA registration for ultrasound imaging devices.This role will support the preparation and compilation of regulatory submissions to ensure timely product approvals in China. · ...