Sr. Program Manager, Quality Assurance/Regulatory Affairs (Hybrid)
Johnson, Kansas
Quest Diagnostics Incorporated
The Sr. Program Manager, Quality Assurance/Regulatory Affairs will lead a variety of large projects or programs within the Quality & Regulatory Affairs organization with special focus on deployment of an enterprise-wide electronic Quality M...
11d
| Job Type | Full Time |
Sr. Program Manager, Quality Assurance/Regulatory Affairs (Hybrid)
Pittsburgh, Pennsylvania
Quest Diagnostics Incorporated
The Sr. Program Manager, Quality Assurance/Regulatory Affairs will lead a variety of large projects or programs within the Quality & Regulatory Affairs organization with special focus on deployment of an enterprise-wide electronic Quality M...
11d
| Job Type | Full Time |
(Contractor) Senior Manager Regulatory Affairs
St. Louis, Missouri
(Contractor) Senior Manager Regulatory Affairs Date: Jun 3, 2025 Location: St. Louis, MO, United States About Curium Curium is the world's largest nuclear medicine company with more than a century of industry experience. We develop, manufac...
11d
| Job Type | Full Time |
Global Regulatory Affairs Manager
Neenah, Wisconsin
About us: At Plexus, our vision is to help create the products that build a better world. Driven by a passion for excellence, we partner with leading Aerospace/Defense, Healthcare/Life Sciences and Industrial companies to design, manufactur...
12d
| Job Type | Full Time |
Sr. Director, Regulatory Affairs
Lincolnshire, Illinois
Sr. Director, Regulatory Affairs Job Location(s) US-IL-Lincolnshire # of Openings 1 Job ID 2024-4181 Category Surgical Robotics Business Travel 25% Overview Find a Better Way... ...to use your skills and experience. This is the time to let ...
12d
| Job Type | Full Time |
Director of Regulatory Affairs CMC
Cambridge, Massachusetts
Who is BlueRock? BlueRock Therapeutics LP is a clinical stage cell therapy harnessing the power of cell therapy to create a pipeline of new medicines for people suffering from neurological and ophthalmic diseases. Two of our novel investiga...
12d
| Job Type | Full Time |
Associate Director Regulatory Affairs CMC
Princeton, New Jersey
About Acadia Pharmaceuticals Acadia is advancing breakthroughs in neuroscience to elevate life. Since our founding, we have been working at the forefront of healthcare to bring vital solutions to people who need them most. We developed and ...
12d
| Job Type | Full Time |
Associate Director Regulatory Affairs CMC
San Diego, California
About Acadia Pharmaceuticals Acadia is advancing breakthroughs in neuroscience to elevate life. Since our founding, we have been working at the forefront of healthcare to bring vital solutions to people who need them most. We developed and ...
12d
| Job Type | Full Time |
Director, Global CMC Strategy (Eye Care)
Oyster Point Pharma, Inc (Delaware corp) At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers p...
12d
| Job Type | Full Time |
Associate Director, Global Regulatory Affairs
Wilmington, Delaware
Overview Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rig...
12d
| Job Type | Full Time |