Regulatory Affairs Specialist - Baldwin

This role collaborates cross-functionally with Quality, Engineering, Clinical, and Manufacturing teams to prepare, submit, and maintain regulatory filings with agencies such as the U.S. FDA, · Assist in the preparation · Ensure the maintenance of regulatory files · ...

The Regulatory Affairs Specialist I will support the day-to-day regulatory activities and operations of assigned projects. · We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. · Qualifi ...

The Regulatory Affairs Specialist provides administrative and technical support to ensure compliance with all FDA and other U.S. and international regulatory requirements. The position establishes and meets timelines corporate objectives to meet timely approval. · This position p ...

The Regulatory Affairs Specialist I will support the day-to-day regulatory activities and operations of assigned projects. · We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. · ...

Amazon Music is innovating at some of the most exciting intersections of music and culture. Join us for the opportunity to influence how Amazon Music engages fans, artists, and creators on a global scale. · ...

+Amazon Music is an immersive audio entertainment service that deepens connections between fans, artists, and creators. · ...

Join us for the opportunity to influence how Amazon Music engages fans, artists and creators on a global scale. · We're looking for a Business Affairs Specialist to join our team in Los Angeles.This role will negotiate with record labels and artist management in support of our or ...

+ Develop and maintain strong relationships with key record labels, promoters and artist representatives · + Negotiate license agreements with record labels and artists · Job summary · This Business Affairs Specialist will negotiate with record labels and artist management in sup ...

This role is pivotal in ensuring product safety and compliance with regulatory standards for medical devices. · Position Overview/Responsibilities for the Regulatory Affairs Specialist: Identify, assess, and communicate product safety risks. · Ensure compliance with global medica ...

This role will focus on supporting the EU's In Vitro Diagnostic Regulation (IVDR) transition activities impacting all products currently CE Marked under the IVD Directive. · ...

The Public Affairs Specialist is responsible for managing and enhancing an organization's public image through strategic communication and outreach efforts. · ...

IDR is seeking a Regulatory Affairs Specialist to join one of our top clients in a remote capacity. · ...

The Regulatory Affairs Specialist will play a key role in ensuring compliance with regulatory standards and guidelines within the FMCG industry. This position supports the Quality & Manufacturing department by overseeing documentation and processes to ensure product safety and ad ...

Job Title: · Regulatory Affairs Specialist II · Join our client's Regulatory Affairs team to support the transition to the EU's In Vitro Diagnostic Regulation (IVDR), impacting all CE-marked IVD products. · ...

The Public Affairs Specialist role involves managing an organization's public image through strategic communication and outreach efforts. · ...

+Regulatory Affairs Specialist II with working knowledge of FDA, and CE marking requirements for IVD products. · +Support the IVDR project by revising assigned technical files. · Update labeling specifications to meet IVDR requirements. · ...

This is a process-based role and will be analyzing images, documents, etc. and will be summarizing and drafting. · Understanding of clearance-related legal and contractual issues, such as intellectual property rights including copyright, trademark, and right of publicity, · produ ...

The Regulatory Affairs Specialist will provide support to the Director of Regulatory Affairs in relation to the Company's regulatory compliance efforts. This includes managing regulatory affairs matters for the company, ensuring compliance with regulatory requirements for Company ...

This role supports the European Union In Vitro Diagnostic Regulation (IVDR) transition activities impacting all Bio-Rad products currently CE-marked under the IVD Directive. · Support IVDR transition projects by revising assigned technical files using the latest approved template ...

The Regulatory Affairs Specialist will support the Director of Regulatory Affairs in regulatory compliance efforts. · Strong understanding of regulatory requirements · Effective research and analytical skills · Strong verbal and written communication skills · ...

The Regulatory Affairs Specialist will develop and maintain product labeling that complies with FDA, FSIS, FNS, · and international regulations.Develop, approve, · and maintain product labeling in compliance with regulatory standardsCreate nutrition facts panels in · compliance w ...