Associate Regulatory Affairs Jobs in USA

Make a meaningful difference to patients around the world. From design to production our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory environments. Working in partnership with external government and regulatory authorities and...

Join the Mitsubishi Motors North America (MMNA) Team!At Mitsubishi Motors NA we are driving innovation quality and excellence in the automotive industry. Our commitment to delivering cutting-edge vehicles goes hand in hand with our dedication to fostering a dynamic and inclusive work environment.Our...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medical devices nutritionals and branded generic medicines. Our 115000 collea...

Hours:Shift Start Time:VariableShift End Time:VariableAWS Hours Requirement:8/40 - 8 Hour ShiftAdditional Shift Information:Weekend Requirements:As NeededOn-Call Required:YesHourly Pay Range (Minimum - Midpoint - Maximum):$53.570 - $69.120 - $77.410The stated pay scale reflects the range that Sharp...

The Lead Regulatory Affairs Specialist will serve as the subject matter expert for the Regulatory Affairs team in matters of regulatory procedures and compliance. The Lead Specialist collaborates with cross-functional teams and key stakeholders to ensure the completion of assigned tasks. This role i...

Were here for one reason and one reason only to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. Weve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we...

Make a meaningful difference to patients around the world. From design to production our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory environments. Working in partnership with external government and regulatory authorities and...

Your work will change lives. Including your own.The Impact Youll MakeLead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications.Influence the regulatory strategy of Recursions development prog...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medical devices nutritionals and branded generic medicines. Our 115000 collea...

Hours:Shift Start Time:VariableShift End Time:VariableAWS Hours Requirement:8/40 - 8 Hour ShiftAdditional Shift Information:Weekend Requirements:As NeededOn-Call Required:YesHourly Pay Range (Minimum - Midpoint - Maximum):$53.570 - $69.120 - $77.410The stated pay scale reflects the range that Sharp...

Your work will change lives. Including your own.The Impact Youll MakeLead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications.Influence the regulatory strategy of Recursions development prog...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare with leading businesses and products in diagnostics medical devices nutritionals and branded generic medicines. Our 115000 collea...

Associate Specialist Regulatory Affairs - LicensingAbout Acrisure:A global fintech leader Acrisure empowers millions of ambitious businesses and individuals with the right solutions to grow boldly forward. Bringing cutting-edge technology and top-tier human support together we connect clients with...

IntroductionWerfen Werfen is a growing family-owned innovative company founded in 1966 in Barcelona Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis Acute Care Diagnostics Transfusion Autoimmunity and Transplant. Through our Original Equipment Manufacturing (OEM...

At Alcon were passionate about enhancing sight and helping people see brilliantly. With more than 25000 associates worldwide we innovate fearlessly champion progress and act with speed to advance global eye health. At Alcon youll be recognized for your contributions supported by an inclusive culture...

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together we support innovation from concept to commercialization offering expertise in regulatory strategy clinical tria...

Position Summary:Are you a mission-driven attorney with a passion for administrative law and regulatory advocacy Do you want to research and analyze cutting-edge statutory administrative and constitutional issues If so Democracy Forward Foundation (Democracy Forward) is looking for a Staff Attorney...

The Device Regulatory Affairs Submission Manager is responsible for leading the planning preparation coordination and submission of regulatory dossiers for medical devices and combination products throughout the product lifecycle. This experienced professional partners with Regulatory Affairs leader...

The Director Regulatory Affairs Device is responsible for combining knowledge of scientific regulatory and business issues to support and drive strategy for regulatory submissions including new applications and amendments renewals annual reports supplements and variations. Has influence and responsi...

The Director Regulatory Affairs Device is responsible for combining knowledge of scientific regulatory and business issues to support and drive strategy for regulatory submissions including new applications and amendments renewals annual reports supplements and variations. Has influence and responsi...