Global Regulatory Affairs Principal Specialist
Fort Worth, Texas
Job Title: Global Regulatory Affairs Principal Specialist Location: Fort Worth, TX, Johns Creek, GA, or Lake Forest, CA Summary of Position: Alcon is looking to hire a Global Regulatory Affairs Principal Specialist to join our Regulatory Af...
9d
| Job Type | Full Time |
Global Regulatory Affairs Principal Specialist
Johns Creek, Georgia
Job Title: Global Regulatory Affairs Principal Specialist Location: Fort Worth, TX, Johns Creek, GA, or Lake Forest, CA Summary of Position: Alcon is looking to hire a Global Regulatory Affairs Principal Specialist to join our Regulatory Af...
9d
| Job Type | Full Time |
Senior Regulatory Affairs Manager, Med Device Software (SaMD/SiMD)
Raleigh, North Carolina
This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organizat...
9d
| Job Type | Full Time |
Associate Regulatory Affairs CMC Director
King of Prussia, Pennsylvania
SUMMARY/JOB PURPOSE: Ensure Exelixis development and commercialized products are manufactured in accordance with approved chemistry, manufacturing and control (CMC) requirements. Provide CMC Regulatory expertise for commercial and developme...
9d
| Job Type | Full Time |
Associate Regulatory Affairs CMC Director
Alameda, California
SUMMARY/JOB PURPOSE: Ensure Exelixis development and commercialized products are manufactured in accordance with approved chemistry, manufacturing and control (CMC) requirements. Provide CMC Regulatory expertise for commercial and developme...
9d
| Job Type | Full Time |
San Rafael, California
Who We Are BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health. Since our founding in 1997, we have applied our scient...
9d
| Job Type | Full Time |
East Hanover, New Jersey
Job Description SummaryThe Global Program Regulatory Manager (GPRM) works with some independence under limited supervision to provide strategic and operational regulatory direction and may support the RA global program team (GPT) representa...
9d
| Job Type | Full Time |
Sr Global Program Regulatory Manager (Associate Director) - Cardio-Renal-Metabolic
East Hanover, New Jersey
Job Description SummaryDirects the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports. Provides strategic product direction to teams on interaction and negotiates...
9d
| Job Type | Full Time |
Boston, Massachusetts
Vertex Pharmaceuticals Incorporated
Job Description General Summary: The Patient Safety Individual Case Safety Report (ICSR) Manager is responsible for performing Individual Case Safety Report (ICSR) processing activities, including narrative writing, event coding, and pursui...
10d
| Job Type | Full Time |
Sr. Principal Regulatory Affairs - CMC
Maple Grove, Minnesota
Upsher-Smith Laboratories, LLC
General Summary (Remote Position) The Senior Principal, Regulatory Affairs Specialist, CMC, will manage and oversee development of regulatory strategies for aspects of project(s) or product(s), filing of applications, and interactions with ...
10d
| Job Type | Full Time |