Regulatory Affairs Jobs in Dublin
1 - 15 of 28
Search Results - Regulatory Affairs Jobs in Dublin
Scholar RockDublin
about the company's approach at and and on LinkedIn.
Summary of Position
The Head of Regulatory Affairs, Europe, is a leadership position that will be responsible for building and leading the regulatory team to develop and implement regulatory...
XeolasDublin
markets. We are now seeking an experienced Regulatory Affairs Specialist as we expand.
Overall Role Objective
The Regulatory Affairs Specialist will report directly to the Regulatory Affairs Manager and be involved in all aspects of regulatory affairs...
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Quanta Consultancy Services LtdDublin
Overview
Associate Director Regulatory Affairs - Ireland, Dublin - 12 Month Contract
Are you looking for the chance to join a life changing pharmaceutical organisation in their mission to continuously drive innovation? We are recruiting...
XeolasDublin
pharmaceutical products for international markets. As we expand our in-house capabilities, we are seeking a skilled Regulatory Affairs Associate to support our regulatory publishing and submission activities.
Role Overview
The Regulatory Affairs Associate...
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Regeneron IrelandDublin
At Regeneron, we're advancing science and medicine to improve lives. We're seeking a talented Regulatory Affairs Manager to join our team and play a pivotal role in supporting EU regulatory activities for oncology drug development.
This is your...
1100 Mylan Pharmaceuticals Inc.Dublin
Manager, Regulatory Affairs Global CMC page is loaded## Manager, Regulatory Affairs Global CMClocations: Northern Cross, Dublin, Irelandtime type: Vollzeitposted on: Vor 13 Tagen ausgeschriebenjob requisition id: R5660220Generics [U.K...
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State StreetDublin
Who are we looking for Head of Ireland Regulatory Affairs is responsible for driving the strategic relationship with the Central Bank of Ireland (CBI) by: building effective relationships with supervision teams; generating insight...
1100 Mylan Pharmaceuticals Inc.Dublin
Cookie Notice**Assistant Manager, Regulatory Affairs CMC (Global) page is loaded## Assistant Manager, Regulatory Affairs CMC (Global)locations: Northern Cross, Dublin, Irelandtime type: Full timeposted on: Posted Todayjob requisition id...
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State Street CorporationDublin
Who are we looking for Head of Ireland Regulatory Affairs is responsible for driving the strategic relationship with the Central Bank of Ireland (CBI) by: building effective relationships with supervision teams; generating insight...
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Gilead Sciences, Inc.Dublin
Affairs (GRA) organization and acts as a critical strategic partner across drug discovery, development and commercial teams. Global TA Regulatory Liaisons develop regulatory strategic options and work closely with cross-functional leaders and regulatory...
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Vitalograph IncDublin
teams such as Data Analyst, Engineering, Software, Data Management and Regulatory Affairs teams.
Responsibilities
Design, develop, and validate biomedical signal processing and AI/ML‑based algorithms to support deployment of objective digital health...
EmbectaDublin
responsible for supporting the various product lines in the $1 Billion embecta diabetes business. The Product Engineer's primary role would be to provide support on a global basis for Product Engineering, working closely with regulatory affairs, marketing...
Mesh BioplasticsDublin
Regulation)
Assist in building ESG and sustainability reporting frameworks
Research international regulatory pathways for market expansion
Ideal backgrounds: Environmental science, regulatory affairs, policy, ESG.
Requirements
A can‑do attitude...
Google Ireland LtdDublin
qualifications: Experience organizing data and applying business context to improve processes or operations. Experience supporting organizations under regulatory settlements or consent decrees (e.g., FTC, SEC, CFPB). Familiarity with compliance regulations...
ICON Clinical Research LtdDublin
activities of internal resources to ensure quality and on-time project deliverables are met. The Project Manager is responsible for maintaining the proper project documentation and ensuring compliance with SOPs and regulatory requirements for clinical trials...
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