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Senior Regulatory Affairs Officer

Thornshaw Recruitment
Dublin (City), Leinster (IE)
Start date
17 Nov 2022
Closing date
17 Dec 2022

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Regulatory Affairs
Full Time
Contract Type
Experience Level
Experienced (non-manager)
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Job Details

My client, a global pharmaceutical company now have a new vacancy for a Regulatory Affairs Officer to join the growing Global Regulatory Affairs team located in Dublin.

Your role will be to prepare, contribute to and support their international registrations and Lifecycle activities for their current and actively growing range of pharmaceutical products.  
•    Acts as responsible Regulatory Team member for assigned regulatory projects  
•    Active member in a busy high quality globally focused regulatory team  
•    Preparation and submit Life-Cycle Maintenance regulatory submissions for EU and global markets   
•    Prepares and/or reviews regulatory documentation for submission to regulatory authorities.  
•    Actively participates and employs effective communication practices with internal customers (CMC, Supply Chain, Quality, Clinical, Medical, Pharmacovigilance and exglobal market Regulatory Managers).  
•    Maintain status reports for assigned projects 
•    Always perform assigned work according to current best good regulatory practice, SOPs and in compliance with current legislation and regulatory guidelines. 
•    Learn, develop and train 
Qualifications & Experience required:

Degree in Pharmacy or life science-related degree plus at least 18 months relevant human pharmaceutical experience with focus on filing and lifecycle maintenance of marketed products in Europe and/or emerging markets  
•    >18 months’ pharmaceutical regulatory experience, focusing on lifecycle maintenance of marketed products in Europe and/or emerging markets (e.g., Variations, renewals, new Marketing Authorisation Applications (MAAs) submissions)  
•    Familiarity of the CTD structure and content 
•    Experience of emerging markets / international RoW markets and regulatory filings 
•    Quality control review of technical/ regulatory documents  
•    Understanding of Regulatory strategy and determination of documentation requirements Compliance with SOPs, Change controls and regulatory best practices  
•    Publishing: eCTD and or NEES  
•    Pharmaceutical artwork review experience  
•    Project management experience - an advantage  
•    Experience of Women’s and/or Men’s healthcare – an advantage 
For further detail email Tina at or call +353 1 2784701 or 087 6811990
Thornshaw Scientific is a division of the CPL Group


Thornshaw Scientific Recruitment has been providing a reputable recruitment service to the Biopharmaceutical, Pharmaceutical, Clinical Research, Medical Device, Food and Healthcare industries for over 15 years.

Our strategic focus has always been to grow the business in a way which has ensured the quality of our service has never been compromised. In 2005 Thornshaw was acquired by Cpl Resources, one of Europe’s most successful recruitment companies.

Find Us
00 353 (1) 278 4671
Barton House
6 Old Dublin Road
Co. Dublin
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