Kingsport, Tennessee
Product Steward Job Requisition ID: 53909 Founded in 1920, Eastman is a global specialty materials company that produces a broad range of products found in items people use every day. With the purpose of enhancing the quality of life in a m...
5h
| Job Type | Full Time |
Senior Manager, Global Clinical Regulatory Lead (East Coast Candidates)
Job Description Summary: The Sr. Manager, Global Clinical Regulatory Lead, is responsible for providing strategic and operational direction for the planning, management, support and execution of regulatory activities for PTC drug products (...
7h
| Job Type | Full Time |
Manager Regulatory Affairs (ACT)
Wayne, New Jersey
With a passion for life Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true di...
10h
| Job Type | Full Time |
CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP (Remote US or Canada)
Baltimore, Maryland
Parexel International Corporation
The CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP provides strategic regulatory guidance to cross-functional project teams responsible for product development and post marketing commitments. The CMC Drug & Device expe...
12h
| Job Type | Full Time |
CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP (Remote US or Canada)
Horsham, Pennsylvania
Parexel International Corporation
The CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP provides strategic regulatory guidance to cross-functional project teams responsible for product development and post marketing commitments. The CMC Drug & Device expe...
12h
| Job Type | Full Time |
CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP (Remote US or Canada)
Glendale, California
Parexel International Corporation
The CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP provides strategic regulatory guidance to cross-functional project teams responsible for product development and post marketing commitments. The CMC Drug & Device expe...
12h
| Job Type | Full Time |
CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP (Remote US or Canada)
Chicago, Illinois
Parexel International Corporation
The CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP provides strategic regulatory guidance to cross-functional project teams responsible for product development and post marketing commitments. The CMC Drug & Device expe...
12h
| Job Type | Full Time |
CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP (Remote US or Canada)
Columbus, Ohio
Parexel International Corporation
The CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP provides strategic regulatory guidance to cross-functional project teams responsible for product development and post marketing commitments. The CMC Drug & Device expe...
12h
| Job Type | Full Time |
CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP (Remote US or Canada)
Kennesaw, Georgia
Parexel International Corporation
The CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP provides strategic regulatory guidance to cross-functional project teams responsible for product development and post marketing commitments. The CMC Drug & Device expe...
12h
| Job Type | Full Time |
CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP (Remote US or Canada)
New York, New York
Parexel International Corporation
The CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP provides strategic regulatory guidance to cross-functional project teams responsible for product development and post marketing commitments. The CMC Drug & Device expe...
12h
| Job Type | Full Time |