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…
Description : The Associate Director/Director, Regulatory Affairs – GDP, provides essential support to the Senior Director in overseeing regulatory activities related to Quality …
Description : The Senior Director, Regulatory Affairs - GDP provides strategic oversight and direction for regulatory activities on a regional and/or global scale. This role enta…
Job Description: As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our…
This position serves as a key member of the Meditrial leadership team, providing strategic direction to the Regulatory & Clinical Affairs teams, and is responsible for the developm…
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here,…
AVP of Regulatory Affairs – MLTC Program Responsibilities: The AVP in collaboration with senior management will be responsible to review, draft, negotiate and process agreements…
This position serves as a key member of the Meditrial leadership team, providing strategic direction to the Regulatory & Clinical Affairs teams, and is responsible for the developm…
hi there, we're amika. a friend to hair, hairstylists, her, him, them, + you. amika means friend in the language esperanto and is a symbol of our belief in the power of community +…
At Getinge we have the passion to perform Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge, our …
Stage Picture: brenntag_other_2.jpg JobTitle: Director Regulatory Affairs and Value Added Services Location: South Plainfield/USA Employment Type: Arbeitnehmer Dire…
Job Title: Sr. Specialist, Regulatory Affairs Location: Columbus, OH Job Type: Full time Req ID: 5929 About Us: As a developer, manufacturer, and supplier of essential me…
Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of internatio…