Director, Regulatory Affairs - Thousand Oaks

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. · ...

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. · ...

This position can be located in Thousand Oaks, CA or the San Francisco Bay Area Reporting to the Vice President of Regulatory, the Director, Regulatory Affairs will support regulatory strategy and lead regulatory execution for the company's development programs ensuring complianc ...

This position can be located in Thousand Oaks, CA or the San Francisco Bay Area and will support regulatory strategy and lead regulatory execution for the company's development programs. · Lead execution and implementation of regulatory strategies to support product development. ...

This role manages the end-to-end US FDA Certificate of Pharmaceutical Product (CPP) process and supports document authentication, dispatch, and archiving activities. · Manage the complete US FDA Certificate of Pharmaceutical Product (CPP) process from drafting through internation ...

In this role as a Sr. Regulatory specialist you will develop and implement medical device regulatory strategies to obtain timely approvals from worldwide regulatory bodies From developing and authoring regulatory submissions to providing critical input on cross-functional project ...

Develop and implement medical device regulatory strategies to obtain timely approvals from worldwide regulatory bodies. · ...

The Regulatory Affairs Manager will be responsible for brands in the North America region, supporting retail, professional and consumer businesses of the Company. The role requires a scientific background with experience in regulatory affairs, compliance and business operations. ...

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 ...

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

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. · ...

The Regulatory Affairs (RA) Analyst is responsible for ensuring compliance of raw material documentation, finished product documentation, and finished product packaging with internal specifications and external regulatory requirements. · Minimum of a BS Degree in Regulatory Scien ...

+Job summary · Liquid I.V. is seeking a Regulatory Affairs (RA) Analyst to ensure compliance of raw material documentation and finished product documentation with internal specifications and external regulatory requirements.+QualificationsMinimum of a BS Degree in Regulatory Scie ...

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 ...

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 ...

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 Head of Regulatory Affairs – Americas is a key leadership role responsible for ensuring compliance, safeguarding product safety, · and enabling innovation across the Americas region. · You will lead a talented team of 10 · , influence strategic decisions, · and ensure that Cl ...

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. · ...