Global Head of Regulatory Affairs - Raleigh

In this critical role you will lead regulatory strategies product submissions and a team of talented regulatory affairs professionals to drive timely product approvals and ensure ongoing regulatory compliance in key markets such as USA EU China and more. · ...

We are seeking a Regulatory Affairs Specialist to support regulatory submissions lifecycle management and compliance activities for pharmaceutical or medical device products. · 2–5+ years of Regulatory Affairs experience (Pharma Biotech or Medical Devices) · Strong knowledge of F ...

We are seeking a Regulatory Affairs Specialist to support regulatory submissions lifecycle management compliance activities for pharmaceutical medical device products. · This is a W2 contract role supporting ongoing regulatory operations in a fast-paced GxP environment. · Prepare ...

Sr. Regulatory Affairs Manager is responsible for developing and executing regional regulatory strategies for QOL initiatives. · ...

The Senior Manager, Regulatory Affairs will develop and execute submission delivery plans for global regulatory submissions such as IND annual reports, clinical trial applications, orphan drug designations, Biologic License Applications, CE marking and other marketing application ...

The Senior Manager Regulatory Affairs will develop and execute submission delivery plans for global regulatory submissions such as IND annual reports, clinical trial applications, orphan drug designations, Biologic License Applications, ...

+The Associate Regulatory Affairs Manager will support the development review and submission of regulatory documents for medical devices and IVD products. · +The Associate Regulatory Affairs Manager will support the development review and submission of regulatory documents for me ...

The Director / Senior Director / Executive Director, CMC Regulatory Affairs is responsible for leading global regulatory CMC development, · ...

Azurity Pharmaceuticals is seeking a Global Head of Regulatory Affairs to oversee regional regulatory leads and staff responsible for ensuring global/regional regulatory strategies are written, reviewed, and executed according to plan. · Oversees regional regulatory leads and sta ...

Azurity Pharmaceuticals is seeking a Global Head of Regulatory Affairs to lead global regulatory strategies and ensure compliance with global regulations. · ...

Support the Senior Director in developing and executing regional regulatory strategies for QOL initiatives within specific regions. · ...

The Senior Manager Regulatory Affairs will develop and execute submission delivery plans for global regulatory submissions such as IND annual reports clinical trial applications orphan drug designations Biologic License Applications CE marking and other marketing applications. · ...

The Senior Manager, Regulatory Affairs will develop and execute submission delivery plans for global regulatory submissions such as IND annual reports, clinical trial applications, orphan drug designations, Biologic License Applications, CE marking and other marketing application ...

Atlantic Medical Management (AMM) is seeking an Regulatory Affairs Assistant to perform responsibilities in support of the Compliance department within AMM. · ...

The Regulatory Affairs Specialist will be responsible for a wide variety of regulatory activities for sustaining products including medical devices and Software as Medical Device (SaMD) and regulatory operation. · ...

Job summaryThe Manager Regulatory Affairs drives key regulatory activities working seamlessly across functions to translate scientific clinical and technical insights into high-quality regulatory submissions while supporting regulatory strategy across the organization. · ...

The Regulatory Affairs Specialist is responsible to develop and execute the regulatory strategy for new product development, design changes, and field safety corrections, · Author EU MDR technical files and will contribute to other international regulatory submissions. · Particip ...

Job summaryThe Regulatory Affairs Specialist is responsible to develop and execute the regulatory strategy for new product development... · ...

The Regulatory Affairs Specialist is responsible to develop and execute the regulatory strategy for new product development, design changes, and field safety corrections, · Author EU MDR technical files and will contribute to other international regulatory submissions. · Particip ...

+The Director of Regulatory Affairs at Pharmaceuticals will work closely with product development core teams and sub teams in setting company goals and work closely with these groups in meeting company goals. · +Bachelor's degree required (advanced degree MS, PhD, PharmD, MD pref ...