Regulatory Affairs Associate - Temecula, CA

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. · ...

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 ...

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. · ...

+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 have a strong understanding of FDA EU and worldwide 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 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 ...

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 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 ...

The Associate Director is responsible for conducting educational grant development followed by content development for awarded grants and cultivating relationships with expert faculty to identify ongoing opportunities. The role requires investigative and analytical skills and hig ...

We are seeking an Associate Director for our team who will be responsible for developing high-caliber medical content with editorial excellence adhering to adult learning principles. · ...

Join Applied Medical as an Associate Specialist in Premarket Regulatory Affairs and help shape the future of medical innovation. · ...

We are looking for a Regulatory Affairs expert to support our US division. · Help with regulatory requirements and prepare regulatory submission for all new/modified combination products. · ...

We currently have an opening for a Principal Clinical Advisor. This role can be located at our Temecula, CA or Santa Clara, CA locations. · Abbott Vascular provides innovative products for treatment of vascular disease. Our portfolio includes drug-eluting stents,bare metal stents ...

The instructor position plays a critical role in the teaching and learning process, ensuring that students achieve mastery of course, program, and institutional learning outcomes. · ...

The instructor position plays a critical role in the teaching and learning process, ensuring that students achieve mastery of course, program, · & institutional learning outcomes. · ...

Abbott es una empresa líder en salud que ayuda a las personas a vivir más plenamente en todas las etapas de la vida. · Nuestra cartera de tecnologías que cambian la vida abarca todo el espectro de la atención médica, con negocios y productos líderes en diagnósticos, dispositivos ...

We are seeking a Principal Clinical Advisor to join our team at Abbott. As a key member of our clinical development team, you will provide clinical knowledge and expertise to support the development of new products and concepts. · Bachelor's degree in a related field or an equiva ...