REGULATORY MEDICAL AFFAIRS PROJECT jobs in CALIFORNIA, United Kingdom

Mammoth BioSciences OPPORTUNITY Mammoth is hiring a Director/Sr. Director, Regulatory Affairs, Therapeutics...-US equivalent Proven track record with regulatory agencies Strong project management skills and drive for excellence Experience...

, and scientists. This Regulatory Affairs Specialist will work out of our Alameda, CA location in the Diabetes Care Division. We’re... as core team member providing review and analysis of applicable regulatory guidelines and project regulatory assessments...

for the treatment of structural heart disease. The Opportunity We are recruiting for a Regulatory Affairs Specialist II... requirements in relation to product development, submissions, product maintenance, project plans. Implements Division Regulatory...

, and scientists. The Opportunity This Regulatory Affairs Specialist II - APAC will work out of our Alameda, CA, location in the... by utilizing team goals and division regulatory priorities. Provides support to Regulatory Affairs management when working...

is a plus (such as RAC from the Regulatory Affairs Professionals Society.) Medical devices and IVD international submissions experience 3-5... sensing technology. The Opportunity As an individual contributor, the function of a Senior Regulatory Affairs Specialist...

, imaging catheters and software, vessel closure devices and peripheral stents. This Regulatory Affairs Senior Manager...-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices...

Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help... medical writing projects in a fast-paced environment with accountability for successful completion within scope of project...

ecosystem to drive better health outcomes. Description As a Senior Regulatory Affairs Specialist, Medical Devices at Verily... Affairs, or related discipline). 8+ years of Regulatory Affairs submissions experience in medical devices, SaMDs, AI/ML...

Regulatory Affairs for Biologics is responsible for leading a matrix team of professionals, who work with a specific product in... Gilead’s global portfolio of biological products in CMC Regulatory Affairs. This position will provide leadership...

. Position Description As an Associate Specialist in Post-market Regulatory Affairs, plays a crucial role in ensuring... that our medical devices continue to meet regulatory requirements and maintain their safety and effectiveness after they have been...

Medical and play a crucial role in revolutionizing medical devices. As a Specialist in Premarket Regulatory Affairs... and understanding of regulatory requirements between project teams and Applied Medical’s global regulatory resources. Performance...

Requirement: 5 years of experience in IVD Regulatory Affairs or Medical Device Regulatory Affairs as a Regulatory Affairs... in IVD Regulatory Affairs or Medical Device Regulatory Affairs as a Regulatory Affairs Specialist, or a related...

Job Description HI-Bio, Inc., a Biogen company, is seeking a Global Regulatory Affairs Lead to develop and implement... will have experience in the immunology space and expertise in global regulatory filings. Reporting to Head of Regulatory Affairs, HI-Bio...

Job Description Summary The Senior Regulatory Affairs Specialist is part of the team responsible for Core Business New...) with desired claims, per project plan. Reviews and supports product design changes through regulatory assessments, and implements...

The Regulatory Affairs (RA) Associate Director, Labeling will be responsible for labeling activities across programs... as required. The RA Associate Director, Labeling will be overall responsible for ensuring compliance with US regulatory requirements...

medical devices. Responsible for activities which lead to and maintain domestic and international regulatory approval... regulatory support on project teams. May provide consultative and training support to the business unit and core regulatory...

Job Description: The Regulatory Affairs (RA) Associate Director, Labeling will be responsible for labeling activities... with US regulatory requirements for labeling, and for coordinating internal labelling activities and processes for regulatory submissions...