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Search Results for Medical Affairs
Job Title. Location Salary Actions

Senior Regulatory Affairs Specialist

Our client is a leading Pharmaceutical organisation based in the West of Ireland. The Senior Regulatory Affairs Specialist will be a member of the Research and Development, Regulatory Science group in a well-established team. The role will be very diverse – always something new to learn. Very interesting products -very dynamic. This role will give experience of dealing with health authorities worldwide & working on maintenance projects as well as new projects. It will also involve the person taking leadership on projects under supervisor’s guidance. Full traini...

Location: Galway,
Senior Regulatory Affairs Specialist
Galway Not Disclosed

Quality Assurance and Regulatory Affairs Manager

Quality Assurance and Regulatory Affairs Manager Our client, one of the largest biomedical innovator based in Dublin is looking to recruit QA/RA Manager wh

Location: Dublin North,
Quality Assurance and Regulatory Affairs Manager
Dublin North Not Disclosed

Consultant

Life Science Recruitment is a specialist recruitment agency with a focus on the recruitment and selection of professionals for the pharmaceutical, biotechnology

Location: Cork,
Consultant
Cork Not Disclosed

Mechanical Design Engineer

Mechanical Design Engineer required to focus on the development of cutting edge medical devices in the Cardiac and Vascular space. Engineers are directly involved in the development of innovative products for use in medical procedures. Principal R&D Engineers are directly involved in all stages of the product development process from concept generation through to commercialization of cutting edge devices such as structural heart devices. Responsibilities: Support basic clinical need through opportunity assessment and device concept to prototype. You will participate in...

Location: Galway,
Mechanical Design Engineer
Galway Not Disclosed

QA Specialist (QC)

This position is responsible for carrying out tasks and projects related to management of Quality Assurance activities at Janssen Biologics as required by Good Manufacturing Practice (GMP). These activities include Incoming material release, Batch release, Change control, Event management, Supplier qualification, Annual product review and Validation compliance activities.Provide support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met. GENERAL SCOPE OF RESPONSIBILIT...

Location: Cork,
QA Specialist (QC)
Cork Not Disclosed