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Responsibilities: The Associate Regulatory Affairs Manager will support the development review and submission of regulatory documents for medical device and IVD products. This role will assist in managing regulatory projects ensuring compliance with FDA ISO 13485 and other global reg المزيد...

Primary Function of PositionThis role will be responsible for providing financial analyses and oversight to the functional executives of the Regulatory Affairs and Quality Assurance (RAQA) organization as they drive both strategic and tactical decision making globally.Such responsibil المزيد...

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 المزيد...

Responsibilities: Perform specialized level work assignments and/or analyses evaluation preparation and submission of documentation for the worldwide regulatory registration ensuring products and procedures comply with regulatory agency specifications. Supports necessary regulatory a المزيد...

Responsibilities: The Regulatory Affairs Associate with minimal guidance prepares reviews and submits high quality annual reports with FDA within Annual report timelines and in accordance with regulatory guidelines and applicable federal laws. With minimal guidance ensure to compile المزيد...

Responsible for technical support and product testing in the US with the objective to support sales and operations in growing the business. Primary focus on laboratory testing and regulatory compliance.JOB FUNCTIONS Provide technical support to sales teams and account managers in المزيد...

Regulatory Affairs Specialist needs 2 years experience Regulatory Affairs Specialist requires: Bachelors Degree in Chemistry Biology Toxicology or related field. Experience in professional level position in business. Experience with OSHA/TSCA/RCRA/Export regulations desirable. Abi المزيد...

POSITION: Senior Regulatory Affairs SpecialistLOCATION: Union City CAWORK SCHEDULE: Full-Time Onsite Our client is seeking an experienced Senior Regulatory Affairs Specialist to join our team and play a key role in supporting regulatory operations across the company. In this role you المزيد...

Work Flexibility: HybridStryker is hiring a Senior Regulatory Affairs Specialist to join our Sage business in Cary Illinois! In this role you will support product compliance and market access by applying your understanding of regulatory frameworks requirements and procedures throughou المزيد...

Job Description:Responsible for assisting with ensuring compliance with US OSHA and Canadian Workplace Hazardous Materials Information System (WHMIS). This includes gathering maintaining and correcting data in to the SAP EHS database for the preparation of Safety Data Sheets (SDSs) pr المزيد...

Job Description: Seeking a Regulatory Affairs Associate to support international addendum labelling (IFUs import labels and country-specific labeling) for medical devices. This role involves collaboration with global RA teams and ownership of labeling compliance processes. Responsibil المزيد...

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 and المزيد...

Who We Are:Galaxy is a global leader in digital assets and data center infrastructure delivering solutions that accelerate progress in finance and artificial intelligence. We believe that blockchain and digital asset innovation will transform how value moves through the world and wer المزيد...

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 المزيد...

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 المزيد...

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 المزيد...

The Global Government Affairs (GGA) team aims to create broad alignment between Visas business objectives and public policies that affect the payments industry. Externally the GGA team engages a wide range of stakeholders to raise awareness of and build support for policies that expan المزيد...

DescriptionAt Ascendis we strive to make meaningful improvements in patients lives. We make business decisions on patients needs and we do our best every day to realize our products benefits for our patients. We are driven by patients science and data. We are dedicated to being curiou المزيد...

Responsibilities: The role includes obtaining and maintaining regulatory approvals supporting quality management system (QMS) objectives and ensuring adherence to applicable regulatory standards. The Regulatory Affairs position is responsible for global product registrations and ensu المزيد...

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 المزيد...