Associate Regulatory Affairs Jobs in USA

Responsibilities: Supports necessary regulatory activities required for product market entry. Preparation of regulatory submissions for Electrophysiology Mapping and Imaging devices to achieve departmental and organizational objectives. Review and approve engineering change orders fo More...

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

Every role at Trove Brands is critical to our successful functioning as a whole. This position is responsible for supporting global compliance efforts for our nutritional supplements foods and related products. This role plays a key part in ensuring regulatory alignment across interna 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 teams as More...

Location: Nashville TN (Hybrid); Remote is available if not local Travel: If working remotely travel is expected once every 1 month to Nashville TN.We are a fast-growing innovative company that is revolutionizing global health. We have a dynamic team that is passionate about improving More...

DescriptionAscendis Pharma is a dynamic fast-growing global biopharmaceutical company with locations in Denmark Europe and the United States. Today were advancing programs in Endocrinology Rare Disease and Oncology.Here at Ascendis we pride ourselves on exceptional science visionary l More...

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 More...

Responsibilities: The Regulatory Coordinator is responsible for the coordination preparation and maintenance of regulatory documentation and compliance for clinical trials. This role ensures adherence to local state and federal regulations including but not limited to FDA ICH and GCP More...

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 More...

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 More...

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 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...

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 More...

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 More...

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 More...

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 More...

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 More...

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 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 and More...