Associate/Associate II, Regulatory Affairs - Yorba Linda

+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 · ...

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

Become part of Southern California Edison's team as a Regulatory Affairs & Compliance Advisor. · Support complex compliance operations · ...

Become a Regulatory Affairs & Compliance Advisor at Southern California Edison (SCE) and build a better tomorrow. · ...

Career-defining. Life-changing. · iRhythm is shaping a future where everyone, everywhere can access the best possible cardiac health solutions. · ...

Develop regulatory submissions and assessments to ensure timely global commercialization of products. · Ensure personal and Company compliance with all Federal State local and Company regulations policies and procedures. · ...

We're looking for innovators who strive to make a difference. We care about our people and our industry of improving the health, well-being and quality of life of individuals with allergic conditions. · Lead by induvial contribution, and direct a team to prepare regulatory submis ...

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 Post-Market Regulatory Affairs Specialist represents the Regulatory Affairs function.The position is responsible for knowledge of requirements and processes for maintaining a product in the clinical setting. · A strong candidate must have Medical Device IDE (clinical trial) e ...

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 · ...

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 ...

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

Responsible for planning, coordinating and implementing regulatory Submissions for products that require government approval. · ...

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

We are searching for a Director of Regulatory Affairs with deep expertise in invasive electromechanical medical devices and extensive experience preparing and submitting · 510(k) notifications. This individual will lead regulatory strategy and submissions for · devices requiring ...

The Manager provides regulatory guidance and strategic direction for Biological and Pharmaceutical Advertising initiatives. · ...

+Job summary · Regulatory Affairs is responsible for planning coordinating and implementing regulatory Submissions for products that require government approval. · +Demonstrates working knowledge of healthcare-related regulations · Demonstrates in-depth knowledge of preparing a s ...

We are a high-growth company with an entrepreneurial spirit that produces reliable products supported by proven clinical data. · - Familiarize with the design manufacture and clinical use of Terumo Neuro products · - Perform specific regulatory tasks for new/modifified product · ...

This role will focus on supporting the EU's In Vitro Diagnostic Regulation (IVDR) transition activities impacting all products currently CE Marked under the IVD Directive. · ...

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 ...