Student Affairs Specialist - Anaheim, CA

At American Career College Educational Foundation we share a passion for students and transforming education As an associate for a certified Great Place to Work you will join a collaborative student centric culture valuing academic integrity mutual respect student learning servic ...

At CJ Schwan's, we don't just make food — we help create moments that matter. · Develop, approve, and maintain product labeling in compliance with regulatory standards · Create nutrition facts panels in compliance with FDA and USDA labeling regulations · ...

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 ...

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 ...

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. · ...

+ 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 ...

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

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. · ...

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 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 Principal Regulatory Affairs Specialist will serve as the company's primary expert for global regulatory submissions, with a strong focus on EU CE Mark and US FDA pathways for cardiac ablation catheters. · ...

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 ...

We are seeking a Regulatory Affairs Specialist to provide regulatory support and expertise for U.S. and global medical device submissions.This role will support execution of global regulatory strategies, ensure compliance with FDA, EU, and international requirements, and collabor ...

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 ...

+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 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 ...

We are seeking a Regulatory Affairs Specialist to provide regulatory support and expertise for U.S. and global medical device submissions. · Provide regulatory support for U.S. and global submissions. · ...

The Regulatory Affairs Specialist will provide support to the Director of Regulatory Affairs in relation to the Company's regulatory compliance efforts. · Assist in managing regulatory affairs matters for the company · Responsible for supporting registration/regulatory needs to m ...

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 ...

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 ...