Director - Rates & Regulatory Affairs - N BLACK CANYON HWY PHOENIX, Arizona, United States

This role develops regulatory strategies for existing, new, and modified medical devices and other (regulated) products. · The individual will also be responsible for mentoring and providing guidance to their direct reports and cross-functional product development teams on US and ...

We have an exciting opportunity for a skilled and experienced FDA Regulatory Affairs Specialist to join our team This position reports to the Sr. · Director, FDA Regulatory Affairs & Food Safety and will support Central animal food facilities. · The position includes interacting ...

We are hiring a Regulatory Affairs Manager to support regulatory activities across a diverse pharmaceutical portfolio. · ...

Prepares regulatory applications and reviews communications to ensure they adhere to applicable regulatory standards. Maintains medical device regulations and supports product release process. · ...

The Associate Regulatory Affairs Manager will support the development review and submission of regulatory documents for medical device and IVD products. · This role will assist in managing regulatory projects ensuring compliance with FDA ISO 13485 and other global regulatory requ ...

Central has an exciting opportunity for a skilled and experienced FDA Regulatory Affairs Specialist to join their team. · ...

We're hiring a Medical Director to join our Clinical Affairs team.You will build and oversee the Clinical Policy Regulatory Compliance functions within the Office of Clinical Affairs. · Lead and grow the Clinical Policy & Regulatory Affairs team. · ...

The Director Regulatory Affairs is responsible for developing and executing the global regulatory strategy for Stryker Sustainability Solutions business unit.Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad ...

The Regulatory Affairs (RA) Specialist will provide primary RA support for one or more product lines and/or region(s), including independent participation on new product development teams and continued RA support through the lifecycle of the product. · We are seeking a highly mot ...

The Regulatory Affairs (RA) Specialist will provide primary RA support for one or more product lines and/or region(s), including independent participation on new product development teams and continued RA support through the lifecycle of the product. · ...

As a Regulatory Affairs Analyst at Caris Life Sciences you will be responsible for regulatory activities related to medical devices/ in vitro diagnostic products including supporting regulatory compliance activities for US and international regions. · ...

Support regulatory activities related to medical devices/in vitro diagnostic products. · ...

This position will serve as the Public Records Custodian and Department Rulemaking Officer. · ...

+Job summary · The Regulatory Affairs Specialist role is responsible for preparing and submitting documentation for FDA 510(k) submissions.++•Ability to work in a fast paced collaborative team environment+•Ability to handle multiple projects and coordinate cross functional teams+ ...

The Regulatory Affairs Associate role is responsible for assisting with preparing and submitting the appropriate documentation for pre-market submissions. · ...

The Regulatory Affairs Engineer is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies. · ...

Under the supervision of the Vice President - Rates & Revenues, plays a critical role in driving Arizona Water Company's regulatory and rates strategy. · ...

The Regulatory Affairs Engineer role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies. · ...

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions. · ...

We are seeking a Regulatory Affairs Analyst to support our medical devices and in-vitro diagnostic products. The successful candidate will have experience in regulated environments and knowledge of domestic and international medical device regulations. · ...