Regulatory Affairs Administrator
Company:
My client is a leading global developer and manufacturer of quality control materials and software for clinical laboratories based in Ballina, Co Tipperary on the Clare/Tipperary border.
Position:
Regulatory Affairs Administrator (Contract basis)
Location:
Killaloe, Ireland
Job Category:
Other
EU work permit required:
Yes
Job Reference:
10fd35a11049
Job Views:
5
Posted:
01.08.2025
Expiry Date:
15.09.2025
Job Description:
* Provide administrative support to regulatory staff, including filing, document tracking, and responding to requests.
* Set up and maintain files, prepare reports, take minutes during meetings.
* Perform data entry, proofread documents, and compile reports.
* Manage incoming and outgoing mail, including courier services.
* Coordinate and manage the regulatory admin inbox.
* Schedule and support meetings.
* Communicate with internal and external stakeholders as required.
* Maintain documentation, plans, reports, schedules, databases, spreadsheets, and logs.
* Assist regulatory staff with submissions to authorities.
* Perform other duties as assigned.
Qualifications:
* Degree in Science, Engineering, or Quality Assurance discipline.
* 1+ years’ experience in a regulated medical product environment is advantageous.
* Knowledge of FDA 21CFR, ISO standards, IVDD 98/79/EC, and other international regulatory requirements.
* Strong communication skills, both verbal and written.
* Attention to detail and ability to prioritize tasks.
How to Apply:
If interested, contact Sarah Jeanne at CPL Limerick or send your CV in confidence.
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