Regulatory affairs specialist Job in Galway, Galway Ireland
JOB DESCRIPTION The Regulatory Affairs Specialist (Pharma) will be responsible for the preparation of and contribution to regulatory submissions for various pharmaceutical products, to worldwide markets. Role and responsibilities:· Life cycle management and regulatory filing maintenance activities;· Preparation, review and submission of supplements to existing approvals (with guidance from Senior Regulatory Specialist/ Regulatory Manager).· Monitoring the progress of regulatory submissions, responding to queries and ensuring that approvals Read more […]
November 23, 2009
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