Assistant General Counsel – Regulatory Affairs - Scottsdale, AZ

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 ...

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). This role also supports post-market regulatory compl ...

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

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. · ...

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

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. · ...

+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 ...

+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 Document Specialist provides support in various projects including formulas labels product materials and records review product registration and helps support the work associated with obtaining government approval for product imports into global markets. · ...

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. · ...

Job Description Summary · The RA Intern provides support for a variety of Regulatory Affairs activities related to global registrations or RA projects. The RA Intern may support multiple Regulatory Affairs professionals across different product lines and may work on a single proj ...

Job Description Summary · The RA Intern provides support for a variety of Regulatory Affairs activities related to global registrations or RA projects. The RA Intern may support multiple Regulatory Affairs professionals across different product lines and may work on a single proj ...

The Regulatory Affairs Document Specialist provides support in various projects including formulas labels product materials and records review product registration and help support the work associated with obtaining government approval for product imports into global markets.The ...

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. · ...

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 ...

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

At Caris, we understand that cancer is an ugly word—a word no one wants to hear, but one that connects us all. That's why we're not just transforming cancer care—we're changing lives. · We introduced precision medicine to the world and built an industry around the idea that every ...

We are seeking an accomplished Regulatory Affairs Manager with hands-on regulatory experience to architect and drive regulatory strategy for our most complex products. · ...

We are seeking an accomplished Regulatory Affairs Manager with hands-on regulatory experience to architect and drive regulatory strategy for our most complex products. This role is pivotal in shaping the regulatory landscape for our portfolio, navigating novel regulatory pathways ...

Job Title: Regulatory Affairs Specialist 1 · Job Location: Mesa, Arizona, Hybrid) · Duration: 12+ months (Contract to Hire ) · Shift: 8 am to 5 pm (8 hour days) · Pay Rate: $38/Hr. on W2 · Job Description: · The Clinical Research Regulatory Specialist is responsible and accountab ...