Associate Regulatory Affairs Jobs in USA

Job DescriptionEMPLOYER: Kraft Foods Group Brands LLCPOSITION: Global Manager FSQ Regulatory Affairs ExportDUTIES: The Global Manager FSQ Regulatory Affairs Export will work within the export regulatory team and be responsible for enabling and reviewing nutritional and regulatory comp More...

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...

Additional Information : Due to the nature of our business and the role please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19.  Details can vary by role.Intuitive is an Equal Opportun 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...

Responsibilities: Regulatory Labelling Documentation. Support the creation and maintenance of assigned labeling projects to enable worldwide regulatory submissions. Independently prepare and maintain the Tracking Sheets for the global regulatory dossiers related to labeling projects More...

Responsibilities: In this role you will perform specialized level work assignments and/or analyses evaluation preparation and submission of documentation for regulatory registration ensuring products and procedures comply with regulatory agency specifications. Supports necessary regu More...

Responsibilities: Responsibilities include developing regulatory strategies reviewing design input/output documentation identification of applicable standards and guidance documents performing regulatory assessments to determine the impact of design/process changes preparing regulato More...

Responsibilities: Preparing documentation for international regulatory registrations. Preparing technical documentation to compliant to MDD and EU MDR. Defining worldwide regulatory requirements are necessary for regulatory approval of products. Participating in cross functional team 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: 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...