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Search Results for Regulatory Affairs for Regulatory Affairs
Job Title. Location Salary Actions

Medical Device Inspector

Medical Device Inspector Our Client an Irish Regulatory Body requires a Medical Device Inspector to join their Medical Device Compliance Team. Responsibilities • Plan and conduct proactive and reactive audits of manufacturers and other economic operators as part of the market surveillance activities for medical devices • Execution of audits relating to designation of notified bodies for medical devices in Ireland and as part of European joint assessment activities • Execution of audits arising from ongoing surveillance and monitoring programme for Notified...

Location: Dublin,
Medical Device Inspector 		Dublin Not Disclosed

Quality Assurance Specialist

JOM AKEM-015176 Quality Assurance Scientist Location: Co. Galway Reporting to Director Innovation Insights. You will be part of the world leader R&D organisation. You will be responsible of the implementation and compliance to relevant quality system regulations and standards for the R&D organization. In particular, you will play a key role in developing, deploying, and maintaining R&D documentatio...

Location: Galway,
Quality Assurance Specialist 		Galway Not Disclosed

Quality Engineer

JOM AECP-463357 Quality Engineer Location Co Louth RESPONSIBILITIES : Manage and provide guidance on Data Strategies for Change Control process Actively supports site CAPA system, mentors associates on CAPA process, co-ordinates preparation of data for CAPA review Meetings etc. Actively supports internal audit program for the site and identify areas of potential noncompliance or improvements. Be a key member of the onsite audit team during external audits, e.g. from Regulatory Authorities and Global Corporate Quality. Assist and facilitate Complaint invest...

Location: Louth,
Quality Engineer 		Louth Not Disclosed

Senior Project Engineer

We’re currently recruiting for an exciting opportunity with an award winning Medical Device organization based in Limerick. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties −Provide engineering support in developing new or improving existing equipment and/or process related activities. −Define or assist in defining process equipment requirements and specifications based on process requirements, safety requirements and customer needs − Perform p...

Location: Limerick,
Senior Project Engineer 		Limerick Not Disclosed

Quality Assurance and Regulatory Affairs Compliance officer

Quality Assurance and Regulatory Affairs Compliance officer Description/summary of role? • Operational and administrative support for the business on all quality assurance and regulatory compliance • Validation of quality processes, quality management systems & administration •&nb...

Location: Sligo,
Quality Assurance and Regulatory Affairs Compliance officer 		Sligo Not Disclosed

Assoc MDR/Vigilance Specialist

We’re currently recruiting for an exciting opportunity with an award-winning medical device organization based in Galway. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. You will be part of a high performing Complaint Handling and Medical Device Regulatory reporting department, which provides value throughout the Product Life cycle through world class execution in Medical Device Reporting and Vigilance compliance. Responsibilities Responsible for the co-ordination of complaint ha...

Location: Galway,
Assoc MDR/Vigilance Specialist 		Galway Not Disclosed

MDR/Vigilance Specialist

We’re currently recruiting for an exciting opportunity with an award-winning Medical Device organization based in Galway. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Duties Responsibilities may include the following and other duties may be assigned. Monitors the company's drug or medical devices surveillance program including the intake, protocol development, evaluation, processing, and follow up on adverse reports, participation in the resolution of any legal liability and in...

Location: Galway,
MDR/Vigilance Specialist 		Galway Not Disclosed
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