Senior Regulatory Specialist - Alameda

The Senior Regulatory Specialist will serve as the regulatory expert within our Quality and Regulatory Affairs team. · Develop and execute strategic regulatory plans for medical devices and combination products development programs across multiple global markets. · ...

We are seeking a Senior Regulatory Specialist to join our Quality and Regulatory Affairs team. This role will drive global regulatory strategies for our medical device and biologic products. · Develop and execute strategic regulatory plans for medical devices and combination prod ...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medic ...

We're a global healthcare leader that helps people live more fully at all stages of life. · This Senior Regulatory Affairs Specialist will work out of our Alameda, CA location in the Diabetes Care Division. · ...

+ Work as Senior Specialist Regulatory Affairs at Abbott in Alameda US for $90k - $180k per year. · Abbott is a global healthcare leader helping people live more fully at all stages of life. · This role provides regulatory input on design and development activities for cross-func ...

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. · ...

The Gas Strategy Regulatory Specialist, Expert is responsible for all aspects of BD&I's regulatory components of our gas strategy to be compliant while supporting innovation in the way we do business. · The position will oversee education of regulatory understanding to better equ ...

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 ...

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 ...

Job Summary: · In addition to the responsibilities listed above, this role is also responsible for: independently scheduling and performing the site reviews, medical record reviews, and Physical Accessibility Review (PAR) surveys; independently conducting site visits for ambulat ...

Job Summary · In addition to the responsibilities listed above, this role is also responsible for: independently scheduling and performing the site reviews, medical record reviews, and Physical Accessibility Review (PAR) surveys; independently conducting site visits for ambulator ...

Job Summary · In addition to the responsibilities listed above, this role is also responsible for: independently scheduling and performing the site reviews, medical record reviews, and Physical Accessibility Review (PAR) surveys; independently conducting site visits for ambulator ...

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 ...

Job Summary · In addition to the responsibilities listed above, this role is also responsible for: independently scheduling and performing the site reviews, medical record reviews, and Physical Accessibility Review (PAR) surveys; independently conducting site visits for ambulator ...

Job Summary · In addition to the responsibilities listed above, this role is also responsible for: independently scheduling and performing the site reviews, medical record reviews, and Physical Accessibility Review (PAR) surveys; independently conducting site visits for ambulator ...

Job Summary: · In addition to the responsibilities listed above, this role is also responsible for: independently scheduling and performing the site reviews, medical record reviews, and Physical Accessibility Review (PAR) surveys; independently conducting site visits for ambulato ...

The Regulatory Affairs Specialist will support regulatory compliance activities by preparing and executing submissions to FDA and other global regulatory agencies. · ...

We're transforming how regulatory documents get written in pharma biotech and medtech through fundamental AI research. · The Role · You'll be teaching AI systems how to think like a regulatory professional evaluating AI-generated content identifying gaps in logic or compliance de ...

+This isn't your typical regulatory affairs position. You'll be teaching AI systems how to think like a regulatory professional. · ...

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 ...