Associate Regulatory Affairs Jobs in USA

Responsibilities: The Regulatory Affairs Manager is responsible and accountable for Company Core Data Sheets (CCDS) Company Core Safety Information (CCSI) and Reference Safety Information (RSI for assigned products including regulatory responsibilities in associated change control an More...

Responsibilities: In this critical role you will lead regulatory strategies product submissions and a team of talented regulatory affairs professionals to drive timely product approvals and ensure ongoing regulatory compliance in key markets such as USA (FDA) EU (MDR) China (NMPA) an More...

Additional Location(s):US-CA-Irvine; US-CA-Valencia; US-MA-Marlborough; US-MN-Maple GroveDiversity - Innovation - Caring - Global Collaboration - Winning Spirit- High PerformanceAt Boston Scientific well give you the opportunity to harness all thats within you by working in teams of d More...

Additional Location(s):US-CA-Irvine; US-CA-Valencia; US-MA-Marlborough; US-MN-Maple GroveDiversity - Innovation - Caring - Global Collaboration - Winning Spirit- High PerformanceAt Boston Scientific well give you the opportunity to harness all thats within you by working in teams of d More...

Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease. A Japan-based company ou More...

Additional Location(s):US-MN-Maple GroveDiversity - Innovation - Caring - Global Collaboration - Winning Spirit- High PerformanceAt Boston Scientific well give you the opportunity to harness all thats within you by working in teams of diverse and high-performing employees tackling som More...

Responsibilities: Preparing documentation for international regulatory registrations. Preparing technical documentation compliant to MDD and EU MDR. Defining worldwide regulatory requirements necessary for regulatory approval of products. Participating on cross functional teams as re More...

Responsibilities: Manages most aspects of company regulatory interface with domestic and international health authorities. Manages the development and deployment of the regulatory program that ensures aggressive product approval. Manages and may generate regulatory submission documen More...

Visa is seeking a lawyer to join its growing Global Regulatory Affairs legal team.  The position will report to a Senior Managing Counsel Global Regulatory Affairs. The role includes responsibility for managing and coordinating complex regulatory matters. The attorney will work c More...

Visa is seeking a lawyer to join its growing Global Regulatory Affairs legal team.  The position will report to a Senior Managing Counsel Global Regulatory Affairs. The role includes responsibility for managing and coordinating complex regulatory matters. The attorney will work c More...

Visa is seeking a lawyer to join its growing Global Regulatory Affairs legal team.  The position will report to a Senior Managing Counsel Global Regulatory Affairs. The role includes responsibility for managing and coordinating complex regulatory matters. The attorney will work c More...

Hybrid Senior Manager Regulatory Affairs - Lincolnshire Illinois Introduction: This is the time to let your talent come to life. Maximize your knowledge and use it for the greater good. Work with top professionals using state-of-the-art technology to improve lives with your innovative More...

Job Description SummaryProvides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch premarket submissions/registrations and post-market compliance working closely with healthcare regulatory bodies globally. Has kno More...

Job DescriptionThis position will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). The primary responsibility for this position is to ensure regulatory compliance for the companys portfolio of medical devices and medical More...

About Scientia Vascular:Our mission is to save lives. Scientia Vascular is aleading innovator and manufacturer of endovascular medical devices. We usemicromachining and microfabrication processes to manufacture products thatprovide physicians with enhanced performance for optimal outc More...

At Alcon we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly champion progress and act with speed as the global leader in eye care. Here youll be recognized for your commitment and contributions and see your career like never before. Together More...

Responsibilities: Support the Senior Director in developing and executing regional regulatory strategies for QOL. initiatives within specific regions. Contribute to providing strategic oversight and leadership to the regulatory team ensuring alignment with company objectives and regi More...

Responsibilities: Prepares and/or coordinate CMC activities for new product registrations post approval changes renewals annual reports and extension applications ensuring on-time and high-quality global submissions. Interface with external Contract Manufacturing Organizations (CMO) More...

Visa is seeking a lawyer to join its growing Global Regulatory Affairs legal team.  The position will report to a Senior Managing Counsel Global Regulatory Affairs. The position is based in Atlanta Austin or Washington D.C. The role includes responsibility for managing and coordi More...

Responsibilities: Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Creates revises and implements quality standards as well as procedures i.e. Standard Operating Procedures (SOPs) etc. for Erbe USAs Quality Management Sy More...