Regulatory Affairs Jobs

California, US residents click here.The job details are as follows: What We DoWe build on the strength of our research and development expertise and a distinctive, entrepreneurial culture that...

Site Name: USA - Pennsylvania - Upper Providence, Durham Blackwell StreetPosted Date: Apr 11 2024We are looking for an ambitious Manager/Associate Director of Regulatory Affairs to ensure the...

The Regulatory Affairs Senior Specialist - Medical Devices coordinates the regulatory activities for development projects including new products and life cycle management. This includes assisting...

Site Name: USA - Maryland - Rockville, USA - Pennsylvania - Upper ProvidencePosted Date: Apr 11 2024Are you looking for a regulatory leadership role where you can build advocacy and accelerate...

About the Department The Lexington Site is home to a growing Development organization, part of Novo Nordisk following its acquisition of Dicerna Pharmaceuticals, Inc. in December 2021. The...

The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territories and to...

About the...

Job DescriptionPosition Title Principal Scientist (Director)DepartmentGlobal Regulatory Affairs and Clinical Safety - Vaccine & Infectious DiseaseBrief Description of PositionThe Regulatory Affairs...

Job DescriptionThe Director, Regulatory Affairs Liaison, is responsible for development and implementation of global regulatory strategy for their assigned projects in the Vaccines and Infectious...

DePuy Synthes, part of Johnson & Johnson MedTech, is recruiting for a Regulatory Affairs Specialist I to support our Spine business. This role is located on-site in Raynham, MA and will work a...

California, US residents click here.The job details are as follows: What We DoWe build on the strength of our research and development expertise and a distinctive, entrepreneurial culture that...

Senior Regulatory Affairs Specialist Location US-Bothell ID 2024-1173 Category Quality Assurance/Regulatory Affairs Position Type Full-Time Work Model Hybrid Company Overview Verathon is a global...

Job DescriptionReports to the Director/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US...

About the Department ...

About the Department The Lexington Site is home to a growing Development organization, part of Novo Nordisk following its acquisition of Dicerna Pharmaceuticals, Inc. in December 2021. The...

IQVIA's Regulatory Affairs Consulting team supports our clients in understanding the regulatory landscape and we play critical roles in supporting market access of innovative medicines (ranging...