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WHAT WE'RE LOOKING FOR:
This is a key US regulatory role to ensure preparation, review and finalization of accurate and timely submissions of all US regulatory documents for medical devices and software driven medical devices. In collaboration with the Senior Regulatory team, this person will participate in meetings and interactions with FDA to establish the regulatory processes for the current and new drug products. This role is the key in ensuring the accurate and the timely submission of all Guerbet regulatory documents, staying current on all US federal regulations to ensure compliance, develop training programs and/or communications documents to meet regulatory requirements, and ensure that regulatory processes are understood and followed.
YOUR RESPONSIBILITES:
YOUR BACKGROUND:
Guerbet is a French based company with a Global reach. Our products and services are made available in more than 80 countries through our affiliates and network of distributors. We offer competitive benefits including but not limited to;
Full Time
Pharmaceutical
$80k-104k (estimate)
04/30/2024
09/26/2024
guerbet-us.com
PRINCETON, NJ
<25
Private
MASSIMO CARRARA
$10M - $50M
Pharmaceutical