Regulatory Specialist - Stanford, CA

The Blood & Marrow Transplantation and Cellular Therapy (BMT-CT) Division is seeking a Clinical Trials Regulatory Specialist II position to support a very active clinical trials faculty. · Prepare regulatory submissions (such as IRB and IND/IDE) and applications and annual report ...

School of Medicine, Stanford, California, United StatesResearchNov 19, 2025 Post Date107768 Requisition # · The Blood & Marrow Transplantation and Cellular Therapy (BMT-CT) Division is seeking a Clinical Trials Regulatory Specialist II position to support a very active clin ...

Meta is seeking an Escalations Specialist to join the Detection, Response, and Intelligence, Regulatory Escalations Team.The team develops bespoke and semi - scaled solutions to escalatory issues. · ...

Meta is seeking an Escalations Specialist to join the Detection, Response, and Intelligence team. The individual will facilitate the resolution of complex high priority escalations by working cross-functionally across different teams. · Serve as an expert on enforcing Meta's Comm ...

A rapidly growing medical device company is seeking a Regulatory Operations Specialist to support global regulatory activities across the product lifecycle. · ...

Picarro, Inc. has an opportunity for a CEMS Regulatory Specialist that will assist the Environmental Solutions team with continuous emissions monitoring systems (CEMS) regulatory reporting and daily quality assurance review. · ...

Responsible for supporting regulatory compliance activities by preparing, assessing, and executing regulatory submissions to FDA, Notified Bodies, and other global regulatory agencies. · ...

Picarro Inc has an opportunity for CEMS Regulatory Specialist that will assist Environmental Solutions team with continuous emissions monitoring systems regulatory reporting daily quality assurance review. · ...

· Title: Regulatory Specialist · Job Location: Remote · Job Term: Full-time · Travel: < 10% · The Opportunity: · Picarro, Inc. has an opportunity for a CEMS Regulatory Specialist to assist the Industrial Solutions team with regulatory reporting for continuous emissions monitor ...

As Principal Regulatory Affairs Specialist at Pulmonx you will drive full spectrum of regulatory activities from initial market authorization through post-market compliance for our US and international device portfolio. · ...

Join a team that plays a key role in bringing life-changing medical technologies to patients around the world. In this role you will ensure global product registrations move efficiently and compliantly through diverse regulatory pathways This is a meaningful opportunity to drive ...

Join a pioneering MedTech company that's transforming cardiac care with innovative solutions. · ...

Join a pioneering MedTech company that's transforming cardiac care with innovative solutions. · ...

Company Description · It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive. As a global leader in robotic-assisted surgery and minimally invasive care, our t ...

Company Description · It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at · Intuitive · . As a global leader in · robotic-assisted surgery · and · minimally invasive ...

Company Description · It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive. As a global leader in robotic-assisted surgery and minimally invasive care, our t ...

Company Description · It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at · Intuitive · . As a global leader in · robotic-assisted surgery · and · minimally invasive ...

The Regulatory Affairs Specialist supports global regulatory strategy and execution for medical device products ensuring compliance with FDA and international regulations throughout the product lifecycle. · ...

A medical device company seeks a Regulatory Operations Specialist for global regulatory activities. · Manage regulatory documentation in electronic document management systems. · Support preparation and submission of regulatory filings. · ...

This Senior Regulatory Affairs Specialist will work out of our Pleasanton, CA location in the Heart Failure Division. As an individual contributor in the function of a Sr. Regulatory Affairs Specialist, you will provide support to the Regulatory Affairs department. With limited s ...