Specialist II, Regulatory Affairs - Santa Clarita

Develops and implements global Regulatory strategies for Class III medical devices This individual will be the Regulatory subject matter expert for all applicable medical devices. · ...

Prepare submissions to obtain and maintain approvals for conducting clinical investigations and for commercially distributing products worldwide. Participate in activities to ensure compliance with worldwide regulatory requirements. · ...

+Prepare submissions to obtain and maintain approvals for conducting clinical investigations and for commercially distributing products worldwide Participate in activities to ensure compliance with worldwide regulatory requirements · +Prepare and maintain global regulatory submis ...

Lief Labs is a premier formulation and product development innovator and manufacturer of dietary supplements. Our in-house product development and R&D team creates the best-tasting and cutting-edge supplement formulations. · The Quality Regulatory Affairs Specialist will be a key ...

Prepare submissions to obtain and maintain approvals for conducting clinical investigations and for commercially distributing products worldwide. Participate in activities to ensure compliance with worldwide regulatory requirements. · ...

The Senior Professional Regulatory Affairs implements and monitors regulatory programs and assists in the homologation of the product range. The Senior Regulatory Affairs (RA) Specialist - International will plan and execute global regulatory activities necessary to obtain and ma ...

We envision a world where everyone can enjoy the delight of hearing.This vision inspires us and fuels our commitment to developing innovative solutions that improve hearing health and human connection - from personal audio devices and wireless communication systems to hearing aid ...

We are seeking a dedicated and talented Director of Regulatory Affairs to join our team.In this role, you will manage all regulatory compliance aspects of our business, ensuring formulas and packaging are compliant with regulations in countries in which products are sold. · ...

We are seeking a dedicated and talented Director of Regulatory Affairs to join our team. · In this role, you will The Director of Regulatory will manage all regulatory compliance aspects of our business, · ensuring formulas and packaging are compliant with regulations in countrie ...

Join Amgen's mission to serve patients living with serious illnesses. · Pioneer in the world of biotech in our fight against the world's toughest diseases. · ...

The Regulatory Affairs Specialist will support the preparation review and submission of regulatory documentation for medical device IVD products ensuring compliance with applicable regulatory requirements including FDA ISO 13485 and other global standards. · ...

We are seeking a dedicated Director of Regulatory Affairs to join our team. · The Director will manage all regulatory compliance aspects of our business. · He/she will work closely with product development, packaging, operations, finance/legal teams. · ...

The Regulatory Affairs Manager will support the preparation and submission of regulatory documentation for medical device products. · ...

As Regulatory Affairs Specialist , you will be responsible for informing both local and global regulatory partners of sustaining changes through the Medtronic Agile system. · This position is an exciting opportunity to work with Medtronic's Diabetes business. ...

Join Amgen's Mission of Serving Patients · As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. · ...

The Regulatory Affairs Manager is responsible for executing regulatory strategies and ensuring compliance with global regulations. This position will provide regulatory input on design and development activities to cross-functional teams. · ...

We anticipate the application window for this opening will close on - 17 Jan 2026 · At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. · ...

This position can be located in Thousand Oaks, CA or the San Francisco Bay Area. The Director Regulatory Affairs will support regulatory strategy and lead regulatory execution for the company's development programs. · ...

We are seeking a dedicated and talented Director of Regulatory Affairs to join our team.DIRECTOR, REGULATORY AFFAIRS (Hybrid) · ...

The Regulatory Affairs Manager will support the preparation review and submission of regulatory documentation for medical device products ensuring compliance with applicable regulatory requirements including FDA ISO 13485 and other global standards. · ...