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 assess ...

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 ...

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 ...

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

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

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 ...

+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 ...

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. · ...

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. ...

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

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. · ...

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. · ...

Looking to change people's lives? Look no further. · ...

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 ...

Provide regulatory guidance in product design, clinical studies, market authorization strategies, labeling. · Review and edit product submissions and other communications prepared by junior department members. · ...

+Job summary · This position is posted by Jobgether on behalf of a partner company. · We are currently looking for a Principal Regulatory Affairs Specialist. · In this role, you will support the development and implementation of long-range regulatory strategies that impact the in ...

We are looking for a Senior Regulatory Affairs Specialist to join our team. The successful candidate will be responsible for ensuring domestic and international regulatory submission and reporting activities are completed in a timely manner. · Prepare domestic and international p ...