Regulatory affairs associate jobs in Bridgewater, New Jersey (NJ) State

Job title: Associate Director, US Advertising and Promotion, Global Regulatory AffairsLocation: Cambridge, MA or Bridgewater, NJAbout the jobThe Associate Director, US Advertising and Promotion serves as the regulatory lead on Review Committees (RCs). As the RC Regulatory Affairs representative, ...

Job title: Associate Director, US Advertising and Promotion, Global Regulatory AffairsLocation: Cambridge, MA or Bridgewater, NJAbout the jobThe Associate Director, US Advertising and Promotion serves as the regulatory lead on Review Committees (RCs). As the RC Regulatory Affairs representative, ...

Global Regulatory Affairs Operation（Sr. This position belongs to Global regulatory affairs department, serving the global Market which encompasses China US, EU, AUS and others. This role requires a detail-oriented professional who can oversee all regulatory affairs and quality assurance activitie...

This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). More Years of direct regulatory affairs experience, including US labeling e...

This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). More Years of direct regulatory affairs experience, including US labeling e...

This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). More Years of direct regulatory affairs experience, including US labeling e...

The Senior Associate, Regulatory Affairs is responsible for supporting applications under pre and post approval conditions. Under the direction of Regulatory Affairs management, participate in drug development from early stage development through final formulation, ensuring compliance with princi...

Minimum 2+ years of experience working in Regulatory Affairs, Product Development, Medical Affairs, or related role within the dietary supplements or food industries. Involves execution of well-constructed regulatory lifecycle maintenance that keep pace with the dynamic supplement and food regula...

D.) preferred Experience Qualifications7 or More Years pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experience ...

Regulatory Affairs Specialist Project Lead I Location: Bridgewater, NJ (Fully Remote) Duration: Contract till Oct 2024 with possibility to extend Fully Remote This role will require direct experience ...

Summary This position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross ...

Represent Regulatory Affairs by attending project team meetings, providing regulatory strategies, reviewing project documentation, and participating in design control activities, as scheduled

Summary The Manager, Regulatory Affairs - Regulatory Project Management (RPM) provides planning and coordination supports for global and US regulatory activities. The Manager RPM is responsible for ...

This role will create and implement effective regulatory strategies to deliver on efficient and robust development plans. The individual will direct, coordinate and implement the preparation of US ...

Summary This position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation of regulatory strategies, work closely with the cross ...

Represents Daiichi Sankyo's regulatory group in internal and external development project meetings. Conduct completeness, scientific accuracy, and ease of review of the submissions. Provides guidance ...

We are looking for a Senior Director - Regulatory Affairs to join our US team. This role is responsible for planning, directing and coordinating regulatory submission activities for sponsors to ...

Summary The Associate Director Global Medical Affairs Oncology (GMA), under the direction of the ... regulations.Collaborates across functions to support GMA MI&E activities in order to achieve ...

Policy Associate Description The policy associate is responsible for supporting all aspects of the ... Track pending legislation in the markets specified by the Dir. of Engineering & Regulatory Affairs

... Medical Affairs departments, ensuring consistency of materials across brands and departments ... LMS) and Regulatory, as needed. ResponsibilitiesEditorial Review of Materials • Review and ...

... ) to support Medical Affairs and HEOR/HTA strategies: Plan, set-up and execute additional ... Contribute, with limited supervision, to documents submitted to Regulatory or Pricing Authorities

... and Regulatory Affairs including the annual report and continued process verification (CPV ... Must provide guidance to other associates in the interpretation of technical issues across an ...

Experience Qualifications 7 or More Years Pharmaceutical industry and Regulatory operations required.4 or More Years regulatory affairs including filing NDA and sNDA. BLA filing to FDA considered a ...

OverviewThe Manager, Regulatory Operations will be responsible for functional activities related to US/Ex-US regulatory submissions. In addition, this individual will be responsible for general ...