Director, Regulatory Affairs - Thousand Oaks

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 ...

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

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 ...

· Position Title: Regulatory Affairs, Manager · Location: Calabasas, California · Reports to: Director, Safety & Regulatory Affairs / Science Policy & Government Affairs · ABOUT THE WELLA COMPANY · Together, WE enable individuals to look, feel, and be their true selves. · Wella ...

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 ...

Job Title: Regulatory Affairs Manager · Onsite 5 days a week. Hard 5pm Stop- Favor work life balance. · Job Description · We are seeking a dedicated and experienced Regulatory Affairs Manager to lead our regulatory submissions, registrations, and licensing documentation efforts. ...

Summary · This role leads global regulatory compliance efforts for a medical device manufacturing organization. You'll manage product registrations and licensing across U.S. and international markets, oversee quality system adherence, and act as the key liaison during regulatory ...

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 ...

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. · ...

Basic Function · The Regulatory Affairs Coordinator will support the Regulatory Department in regulatory compliance-related documentation. They will work closely with the Regulatory Affairs Manager and Specialist to communicate any issues. The coordinator will work with internal ...

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

Job Title: Regulatory Affairs Manager · Onsite 5 days a week. Hard 5pm Stop- Favor work life balance. · Job Description · We are seeking a dedicated and experienced Regulatory Affairs Manager to lead our regulatory submissions, registrations, and licensing documentation efforts. ...

At Beyond - The Plant Protein Company, we started with simple questions. Why do you need an animal to create meat? Why can't you build meat directly from plants? Thus, we make plant-based meats that allow families to eat more, not less, of the traditional dishes they love while f ...

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 ...

Basic Function · The Regulatory Affairs Coordinator will support the Regulatory Department in regulatory compliance-related documentation. They will work closely with the Regulatory Affairs Manager and Specialist to communicate any issues. The coordinator will work with internal ...

· About Liquid I.V. · This job description indicates in general the nature and levels of work, knowledge, skills, abilities and other essential functions expected of the role. It is not designed to cover or contain a comprehensive listing of activities, duties or responsibilitie ...

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. · ...