Pittsburgh, Pennsylvania
Job Highlights Prepare, execute and coordinate Registration Projects in Canada and U.S. for biocidal products (EPA) - Environmental Protection Agency, (FIFRA) - Federal Insecticide, Fungicide and Rodenticide Act and Health Canada (PMRA) - P...
22d
| Job Type | Full Time |
Marlborough, Massachusetts
Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit- High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and h...
23d
| Job Type | Full Time |
Senior Manager, Regulatory Affairs
New York
The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemist...
24d
| Job Type | Full Time |
Senior Manager, Regulatory Affairs
Newark, New Jersey
The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemist...
24d
| Job Type | Full Time |
Senior Manager, Regulatory Affairs
Florida
The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemist...
24d
| Job Type | Full Time |
Executive Director, Regulatory Affairs
Boston, Massachusetts
JOB TITLE: Executive Director, Global Regulatory Affairs DEPARTMENT: Regulatory Affairs REPORTS TO: Vice President, Regulatory Affairs / Sr. Vice President, Regulatory Affairs LOCATION: Boston, MA DATE PREPARED: March 27, 2026 JOB SUMMARY: ...
24d
| Job Type | Full Time |
Director, Nonclinical Safety Assessment Expert (Multiple Therapeutic Areas)
Cambridge, Massachusetts
Job Description SummaryInternal Title: Director #LI-Hybrid Location: Cambridge, MA or San Diego, CA In this key role you will provide global, end to end nonclinical safety leadership across multiple therapeutic areas and modalities, ensurin...
25d
| Job Type | Full Time |
Rochester, New York
Responsibilities We are hiring a Regulatory Affairs Lead within our Kodak Pharmaceuticals group in Rochester, NY. This individual is responsible for establishing, managing, and executing regulatory strategies to support a growing medical de...
25d
| Job Type | Full Time |
Associate Director, Regulatory Affairs Project Planning & Coordination
South San Francisco, California
About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio include...
26d
| Job Type | Full Time |
Sr. Manager, Regulatory Affairs, CMC
Cambridge, Massachusetts
Overview: The Senior Manager, Regulatory Affairs CMC Development is responsible for implementation of the global regulatory CMC strategy for developmental programs. This role will play a critical part in shaping regulatory strategies for em...
26d
| Job Type | Full Time |