Regulatory Affairs Specialist - La Palma

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 · ...

As an associate at American Career College Educational Foundation you will join a collaborative student-centric culture valuing academic integrity mutual respect student learning service responsiveness innovation diversity and stewardship Guiding students to change their own live ...

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 ...

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 ...

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. · ...

The Post-Market Regulatory Affairs Specialist represents the Regulatory Affairs function.The position is responsible for knowledge of requirements and processes for maintaining a product in the clinical setting. · A strong candidate must have Medical Device IDE (clinical trial) e ...

The Regulatory Affairs Specialist is responsible for planning, coordinating and implementing regulatory Submissions for products that require government approval. · Demonstrates working knowledge of healthcare-related regulations · Demonstrates in-depth knowledge of preparing a s ...

We are seeking a Regulatory Affairs Specialist (RAS) with strong IVD experience to support the transition from IVDD to IVDR. This role is responsible for revising and maintaining IVD technical documentation, supporting IVDR labeling conversions, and managing regulatory notificati ...

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 ...

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. · ...

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 ...

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

This position does require 2 days in the office, and this position requires 70% of traveling to community events, job fairs, and other outreach events.In this role, you will help write and edit a variety of public-facing communications products, · such as articles and talking poi ...

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. · ...

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

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. · ...

Regulatory Affairs Specialist · Plan, coordinate and implement regulatory submissions for healthcare products requiring government approval. · ...