Key Responsibilities:
Support Global Regulatory Affairs with national regulatory information and advice as required.
Ensure all medicinal product registrations are current and marketed in full compliance with their approved registration files.
Provide input to the global regulatory affairs databases to ensure up-to-date status regarding national regulatory activities.
Preparation, submission, and follow-up of medicinal product applications, as required and directed, to the HPRA and associated liaison with Global Regulatory Affairs.
Requirements
A 3rd level science qualification
Approx 1-3 years work experience in a compliance environment
Knowledge of EU and national regulatory requirements.
Ability to process technical information.
Accuracy and excellent attention to detail.
Excellent organisational skills.
Strong verbal and written communication skills.
Good interpersonal skills.
For full details contact Tina tdunne@thornshaw.com or call +353 1 2784701 or 087 6811990
Thornshaw Scientific is a division of the CPL Group. www.thornshaw.com
