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Job Title. Location Salary Actions

Controls Engineer

Controls Engineer Our client a multi-national medical device company currently seeks a Controls Engineer to join their team on a contract basis Role/Responsibilities Develop PLC software for new and existing equipment. Visual Basic (VB.net) programming for Machine Control including integrating VB with Motion Control, Digital and Analogue I/O, PLC's, and Vision Applications. Design, development and administration of SQL databases to support manufacturing systems. Develop 21 CFR part 11 compliant applications Design control sy...

Location: Sligo,
Controls Engineer
Sligo Not Disclosed

Clinical Trials Advisor

Clinical Trials Advisor Responsibilities: -Analysis of clinical trial protocols and other client source material -Build up a thorough knowledge of the trial -Preparation of study materials for development teams; -Determine what elements are important to the target audience and the depth of coverage required in the product -Script product content to meet client requirements and in-house quality Standards -Identify leverage from previous trials -Resolve clinical queries from the development teams -Storyboard with Graphic Designers as part of graphic development -Review and sig...

Location: Limerick,
Clinical Trials Advisor
Limerick Not Disclosed

Product Manager - Pharmaceutical

My client is a leading pharmaceutical company based in Ireland. They are seeking a product manager with a minimum of 3 years product management experience in the pharmaceutical sector to join the team. The role will be a 50:50 split between pure marketing and portfolio management. The ideal therapuetic area experience would be analgesics or pain medicine. To discuss the role in more detail and for salary and company information please contact Eamonn O'Raghallaigh MSc on 01 6854848

Location: Dublin,
Product Manager - Pharmaceutical
Dublin Not Disclosed

Pharmacovigilance Specialist

Pharmacovigilance Specialist Our client, a Consultancy based in Munster, is seeking a PV Specialist to join their organisation on a permanent basis. Responsibilities: To complete the duties of a Qualified Person and/or Deputy (QPPV) Writing of Periodic Safety Update Reports and searching for ADRs Assessing adverse reactions for potential signals Producing summary safety tables for Client review Preparation and training for Regulatory Inspections MedDRA coding Understand...

Location: Tipperary,
Pharmacovigilance Specialist
Tipperary Not Disclosed

PhD Studentship - The effect of sacral neuromodulation on inputs to the somatosensory cortex

PhD - The effect of sacral neuromodulation on inputs to the somatosensory cortex

Location: Dublin South,
PhD Studentship - The effect of sacral neuromodulation on inputs to the somatosensory cortex
Dublin South See description