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Your search generated 126 results
The Trade Desk

Senior Product Manager, Regulatory Compliance & Data Governance

Denver, Colorado

The Trade Desk

The Trade Desk is changing the way global brands and their agencies advertise to audiences around the world. How? With a media buying platform that helps brands deliver a more insightful and relevant ad experience for consumers - and sets a...

Job Type Full Time
Masimo Corporation

Vice President, Regulatory Affairs - Outside the U.S. (OUS)

Irvine, California

Masimo Corporation

The Vice President, Regulatory Affairs - OUS is responsible for developing and executing Masimo's regulatory strategy across all regions outside of the United States. This includes managing product submissions, registrations, renewals, and ...

Job Type Full Time
Benjamin Moore & Co

Regulatory Affairs Manager (EU/UK)

Montvale, New Jersey

Benjamin Moore & Co

Regulatory Affairs Manager (EU/UK) ID 2025-2099 Category Legal Position Type Salaried Remote No Starting From USD $127,300.00/Yr. Maximum Pay Range USD $150,000.00/Yr. Shift Time 40 Overview Company Overview At Benjamin Moore, our success i...

Job Type Full Time
New
BioCryst Pharmaceuticals

VP, Global Regulatory Affairs

Durham, North Carolina

BioCryst Pharmaceuticals

Description COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with complement-mediated and other rare diseases. For over three decades we've been guided by our passion for not settling for "ordinary" i...

Job Type Full Time
New
Masimo Corporation

Director, Regulatory

Irvine, California

Masimo Corporation

Job Summary In this high profile role, the Director or Associate Director, Regulatory Affairs will be an integral part of the regulatory affairs team with the responsibility to support the strategic and organizational direction of the regul...

Job Type Full Time
Vanda Pharmaceuticals Inc.

Associate Director, CMC Regulatory

Washington, D.C.

Vanda Pharmaceuticals Inc.

Description Job Responsibilities: Review drug substance and drug product information for completeness and up to current regulatory standards Prepare CMC sections for drug substance and drug product information/data Review relevant FDA/EMA/I...

Job Type Full Time
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