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CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious medical conditions. ...
Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC Submissions Management in Lexington, MA to establish global submission activities ...
Takeda Development Center Americas, Inc. is seeking a Manager, Global Regulatory Affairs CMC Submissions Management in Lexington, MA to establish global submission activities ...
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be ...
Join a Legacy of Innovation 110 Years and Counting! Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards ...
Our Company Explore how you can contribute at AmeriLife. For over 50 years, AmeriLife has been a leader in the development, marketing and distribution of annuity, life and ...
At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four ...
Director, Global Regulatory Affairs, Precision Medicine page is loaded Director, Global Regulatory Affairs, Precision Medicine Apply locations United States - California - ...
Associate Director, Global Regulatory Affairs Labeling in Basking Ridge at Daiichi Sankyo Join a Legacy of Innovation 110 Years and Counting! Daiichi Sankyo Group is dedicated ...
Takeda Development Center Americas, Inc. is seeking a Manager, Regulatory Affairs CMC in Cambridge, MA to Develop the Global Regulatory Strategy for products in commercial ...
Job Title: Director Regulatory Affairs, CMC Location: Bothell About Us: Immunome is a clinical stage biotechnology company headquartered in Bothell, WA dedicated to developing ...
About the role: At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D ...
**HOW MIGHT YOU DEFY IMAGINATION?** Youve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge youve worked hard to acquire ...
The Director/Sr Regulatory Affairs will lead the overall CMC Regulatory strategy for Adverum's gene therapy program/s. This individual will be the key interface between the ...
Press Tab to Move to Skip to Content Link Select how often (in days) to receive an alert: Senior Director, Global Regulatory Affairs Development Pipeline, Cell Therapy Open ...
Would you like to be part of a global biopharma company? Hansa Biopharma is a global, commercial-stage biopharmaceutical company, pioneering the development and commercialization ...
About the Role The Associate Director, US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the Rare Disease, Rare ...
About the Role The Associate Director, US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the Rare Disease, Rare ...
Site Name: USA - Pennsylvania - Upper Providence, GSK House, Switzerland - Zug, USA - Massachusetts - Waltham, USA - North Carolina - Durham Posted Date: May 17 2024 Purpose Ensure ...
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