VP of Regulatory of Affairs - Temecula

We are looking for a "Regulatory Affairs Associate" to join one of our Fortune 500 clients. · Basic knowledge of US and EU medical device regulatory requirements · Experience supporting OUS/international registrations; experience with change management and regulatory impact asses ...

We are looking for a Regulatory Affairs Associate to join one of our Fortune 500 clients. · Basic knowledge of US and EU medical device regulatory requirements · Experience supporting OUS/international registrations; experience with change management and regulatory impact assess ...

We are looking for a Regulatory Affairs Associate to join one of our Fortune 500 clients. · Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval. · ...

The Vice President of Regulatory Affairs is a senior executive responsible for developing, implementing, and leading the organization's regulatory strategy across all products, services, and clinical operations. · ...

+We are looking for a Regulatory Affairs Associate to join one of our Fortune 500 clients. · +Filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval. · Authoring and submitting PMA s ...

Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval.Authoring and submitting PMA supplements (30-day Notice, Real-Time Reviews, 180-Day Supplements, Annual Reports ...

Responsible for filing necessary applications and handling all government interactions pertaining to the regulation process for products requiring governmental approval. · ...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medic ...

The Regulatory Affairs Support role assists regulatory teams in preparing, submitting and maintaining regulatory documentation to ensure compliance with applicable regulations and internal quality standards. ...

+Job summary · We are seeking a Regulatory Affairs Associate to support U.S. and global regulatory submissions for medical device products.This role will assist in executing global regulatory strategies, preparing and maintaining registration dossiers, and ensuring compliance wit ...

The Regulatory Affairs Associate will be responsible for managing regulatory affairs related to medical devices. · The ideal candidate should have direct experience in medical device regulatory affairs with recent hands-on EU MDR 2017/745 experience, · a Bachelor's Degree in phar ...

Regulatory Affairs Associate II job in San Clemente requiring a Bachelor's Degree in pharmacy or related subject and RAC Certification. Proven strong understanding of FDA and EU submission requirements. · ...

Direct medical device regulatory experience with recent hands-on EU MDR 2017/745 experience and FDA interaction required. · ...

We are seeking a Regulatory Affairs Associate II to support medical device regulatory activities with a strong focus on EU MDR compliance.Ensure regulatory readiness and successful submissions across global markets. · ...

We are seeking a Regulatory Affairs Associate to support U.S. and global regulatory submissions for medical device products. · Prepare and manage U.S. and global regulatory submissions, including FDA and CE technical documentation · Support execution of global regulatory strategi ...

The Regulatory Affairs Associate will have a strong understanding of FDA EU and worldwide submission requirements. · ...

Key responsibilities: · Lead the regulatory strategy for new product development and market entry, including 510(k), PMA, and CE Mark submissions. · Prepare, review, and manage regulatory submissions to global authorities such as FDA and EMA. · Collaborate cross-functionally with ...

The Sr. Specialist, Regulatory Affairs will create, evaluate and execute domestic and international regulatory tasks related to global submissions, technical file compilation, · facility registrations and strategy to drive market growth worldwide.Create, evaluate and execute dome ...

+Job summary · The Sr. Specialist, Regulatory Affairs will create, evaluate and execute domestic and/or international regulatory tasks related to the following: global submissions, technical file compilation, facility registrations, special projects and strategy to drive market g ...

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Regulatory Affairs Specialist - REMOTE. · We appreciate your interest and wish you the bestAssist with the implementation of global regulatory roadmaps and marketing strategies. · ...