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Search Results for Medical Affairs
| Job Title. | Location | Salary | Actions |
Supplier Quality Data AnalystSupplier Quality Data Analyst POSITION SUMMARY: The Supplier Quality Data Analyst develops, implements, and maintains supplier databases and collects and analyses supplier quality data in preparation for generation of statistical and analytical reports. PRINCIPAL RESPONSIBILITIES: • Develop and implement supplier databases, data collection systems, data analytics, and other strategies that optimize statistical efficiency and supplier quality. • Collect, analyze, interpret, and summarize supplier quality data in preparation for generation of sta...Location: Westmeath, |
Westmeath | Not Disclosed | |
Clinical Development Associate**This role is exclusively with Life Science Recruitment** Our client is a start-up medical device organisation based in north Dublin. This hiring manager for this role is very highly-regarded in the industry and the successful individual can expect to learn a lot about medicla device clinical development and clinical programme management in a short space of time. Purpose of the role: To support the execution of our client's clinical development plan by delivering first in class projects. Job Responsibilities: This role will provide scientific and technical support to the ...Location: Dublin, |
Dublin | Not Disclosed | |
Senior Regulatory Affairs SpecialistSenior Regulatory Affairs Specialist Job purpose: The Sr. Regulatory Affairs Specialist will develop strategies for complex projects and issues related to regulatory processes, compliance activities, documents, submissions, investigations, product development planning and regulatory agency interaction. The Sr. Regulatory position will assist in mentoring and development of staff members as part of the role. Key responsibilities: • Key responsibilities will include (but are not limited to) the following: • Support global regulatory projects,...Location: Westmeath, |
Westmeath | Not Disclosed | |
Regulatory Affairs Specialist - CN001Regulatory Affairs Specialist Summary Our client is a large Medical Device organisation based in Athlone. They wish to recruit a Regulatory Affairs Specialist who will be responsible for determining and supporting the regulatory activities which lead to, and maintain regulatory compliance and approval for medical products globally Key responsibilites • Apply technical solutions to problem solving • Apply technical solutions to quality improvement projects • Use technical writing skills to clearly describe technical information • Analyze custo...Location: Westmeath, |
Westmeath | Not Disclosed | |
Regulatory Affairs ManagerRegulatory Affairs Manager Our client is an international pharmaceutical discovery organisation and they are currently recruiting for a Regulatory Affairs Manager to join their team on a permanent basis. The ideal candidate will be a dynamic individual, who is self-driven, organized and capable of working on their own initiative in a start-up environment. Responsibilities • Coordinate, prepare and be accountable for all regulatory affairs related activities such as clinical trial applications, organization and preparation of regulatory advice meetings and compilation...Location: Dublin, |
Dublin | Not Disclosed | |
QA Senior Associate (Contract)Plant QA Snr Associate Level 4 Dun Laoghaire Overview: The Plant Quality Assurance (PQA) Snr Associate will typically report to a QA Senior Manager and is a core member of the site Quality Assurance team. The PQA Snr Associate will serve as Quality point of contact for manufacturing operations. The site is focused on continuous improvement of all work processes and practices, therefore in addition to routine Quality Assurance duties, PQA Snr Associates may be asked to carry out additional work functions to support site continuous improvement activities. A...Location: Dublin, |
Dublin | Not Disclosed | |
Head of Quality & Regulatory AffairsHead of Quality & Regulatory Affairs Our client a multinational healthcare company currently seeks Head of Quality and Regulatory Affairs. Reporting to GeLocation: Dublin, |
Dublin | Not Disclosed |
Regulatory Affairs Officer Regulatory Affairs Medical Affairs Microbiology Engineering Biopharmaceutical Engineering QA Specialist Clinical Research Medical Device Westmeath Scientific Quality Assurance Pharmaceutical Regulatory Affairs Clinical Research Regulatory Affairs Regulatory Affairs Consultant Quality Manager Dublin Senior Regulatory Affairs Officer Life Science Regulatory Affairs Specialist Life Science Regulatory Affairs Manager Regulatory Affairs Executive Biotechnology Chemistry
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Regulatory Affairs | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: info@regulatoryaffairs.ie
Copyright © 2012 Life Science Recruitment Ltd
This site uses cookies. For more information on our cookie policy read our Privacy Policy | Terms of Use
Registered as a private limited company. No: 445328 | Web Design / SEO by WebScience | Valid XHTML - CSS
Regulatory Affairs | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: info@regulatoryaffairs.ie
Copyright © 2012 Life Science Recruitment Ltd
This site uses cookies. For more information on our cookie policy read our Privacy Policy | Terms of Use
Registered as a private limited company. No: 445328 | Web Design / SEO by WebScience | Valid XHTML - CSS






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