Director - Rates & Regulatory Affairs - Phoenix

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 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. · ...

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 ...

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

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. · ...

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

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

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. · ...

We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: What would I do if this patient were my mom? · Provide supp ...

+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 (i.e. FDA 510(k) submissions, Health Canada Device License Applications). · +Minimum of Bachelor's degree preferably in Engin ...

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

The Regulatory Affairs Engineer role involves preparing and submitting documentation for FDA clearance and international regulatory bodies. · ...

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies. This position requires a minimum of five years medical device regulatory experi ...