Intern, Regulatory Affairs - Aliso Viejo

+Be at the forefront of innovation – shape regulatory strategies that bring breakthrough therapies and life-changing technologies to patients around the world. · ...

We're a high-growth company, customer-focused with an entrepreneurial spirit producing some of the most reliable and technologically advanced products supported by proven clinical data. · ...

We're seeking an experienced Regulatory Affairs professional to lead global product submission and compliance activities for Class II/III medical devices in the neuro and peripheral space. · ...

Be at the forefront of innovation – shape regulatory strategies that bring breakthrough therapies and life-changing technologies to patients around the world. · ...

Are you interested in working for an organization that is making a difference in people's lives every day? · ...

We are a high-growth company looking for an intern in Regulatory Affairs to join our team. · The Regulatory Affairs team is responsible for executing regulatory strategies and obtaining approvals for our products. · This internship will provide valuable experience and skills in r ...

Responsible for establishing preparing and leading the strategy for worldwide product approval submission activities As a recognized expert manage multiple large projects or processes Responsible for submission activities focused on USEUCanada and for ensuring compliance to FDA a ...

Are you interested in working for an organization that is making a difference in people's lives every day? We're a high-growth company · ...

The position of Principal Regulatory Affairs is responsible for establishing and leading the strategy for worldwide product approval submission activities. This involves managing multiple large projects or processes. · ...

Planifica, coordina e implementa la presentación de solicitudes regulatorias para productos que requieren aprobación del gobierno. · ...

+Responsible for planning coordinating and implementing regulatory submissions for products requiring government approval. · Demonstrates working knowledge of healthcare-related regulations · Demonstrates in-depth knowledge of preparing a submission · ...

Responsible for preparing strategy for worldwide product approval submission activities focused on US/EU/Canada and ensuring compliance to FDA and international regulatory agency requirements. · As a contributing member on product development and operation teams. · ...

We are seeking a Regulatory Affairs Specialist to provide regulatory support and expertise for U.S. and global medical device submissions.This role will support execution of global regulatory strategies, ensure compliance with FDA, EU, and international requirements, and collabor ...

The job description is for a Sr. Specialist, Regulatory Affairs position at MicroVention. The role involves preparing strategy for worldwide product approval submission activities focused on US/EU/Canada and ensuring compliance to FDA and international regulatory agency requireme ...

We are seeking a Regulatory Affairs Specialist to provide regulatory support and expertise for U.S. and global medical device submissions. · Provide regulatory support for U.S. and global submissions. · ...

We are seeking a Regulatory Affairs Specialist (RAS) with strong IVD experience to support the transition from IVDD to IVDR. This role is responsible for revising and maintaining IVD technical documentation, supporting IVDR labeling conversions, and managing regulatory notificati ...

Responsible for preparing strategy for worldwide product approval submission activities focused on US/EU/Canada and ensuring compliance to FDA and international regulatory agency requirements for Neurovascular and Peripheral devices. · ...

Responsible for preparing strategy for worldwide product approval submission activities focused on US/EU/Canada and ensuring compliance to FDA and international regulatory agency requirements. · Execute the approved global regulatory strategy for the assigned market(s). · Analyz ...

The Associate Principal is responsible for establishing and preparing strategy for worldwide product approval submission activities focused on US/EU/Canada and ensuring compliance to FDA and international regulatory agency requirements. · Bachelor's degree in a scientific or tech ...

The position requires a Regulatory Affairs Specialist to plan and implement regulatory submissions for medical devices. The ideal candidate should have mid-level experience and knowledge of healthcare-related regulations. · ...