Senior Quality Engineer (€650000 per annum) / Ireland

Senior Quality Engineer Are you a Quality Engineer looking for an exciting new challenge? The client is currently helping a World-Leading Medical Device company to develop their new Research and Development function in Ireland.

What’s on offer?

• €75,000
• Excellent benefits package, including relocation assistance for the right candidate
• A great opportunity to join a market-leading Medical Device business – driving innovation and providing strategic quality advice to a growing Quality and Engineering team.

The client are a global Medical Device business who are continuing to develop their  presence in Ireland. As part of this growth, the company have committed to a programme of investment in the region that will help develop and drive innovation across their product range.

The Role:

As Senior Quality Engineer, you will be a highly visible member of the Site’s Quality Team and will have responsibility for driving best practice across the business. In addition, you will have specific responsibility for:

• Maintaining Product Quality, Documentation, Compliance, Patient Safety and customer satisfaction to a wide variety of products at different stages of the product lifecycle.
• Ensuring Quality Management and Quality Engineering is at the heart of the business – advising on strategic developments and ensuring products maintain compliance with all relevant standards, including ISO13485 and ISO14971
• Playing a leading role across diverse project teams (including Project Management, Research and Development, Regulatory Affairs, Marketing etc) to manage design change programmes and developing closer relationships between other quality functions to elevate the position of the quality team across the business
• Writing Project Quality Plans in support of the above and writing and developing Risk Management activities across the business.

The Candidate:

The successful candidate is likely to be operating as a Senior Quality Engineer in a Medical Device business at the moment, however there are key skills that you’ll be able to demonstrate:

• Substantial previous experience (5+ Years)  of Quality Engineering within Medical Devices is essential
• An ability to provide strategic Quality advice to a wide range of Senior Stakeholders is essential
• Understanding and knowledge of ISO13485 and ISO 14971 is essential
• Knowledge of validation and reliability testing is preferable but not essential
• Given the nature of the opportunity, our client are able to provide relocation support to the right candidate, however the preference is to identify someone who is currently within Ireland or the EU.