Job Description

Senior Supplier Quality Engineer - North Dublin

Ref No: AM18441

County Dublin, Republic of Ireland

Competitive salary

Senior Supplier Quality Engineer - North Dublin.

Key tasks and responsibilities:
• As a key member of the team, you will be part of a highly innovative Production and Quality network working to deliver high quality product.
• Act as a key liaison and knowledge transfer champion among Supplier Quality, Quality Assurance, Manufacturing Engineering, R&D, Production and Documentation Control.
• Assess suppliers’ capability to meet quality requirements based on data analysis and supplier audit. As a follow-on activity create concise reports that enable project teams to implement improvements and corrective actions.
• Use statistical analysis to support suppliers and drive regulatory standards of excellence. Develop world-class supply chain processes to suit a low volume, high complexity multi-technology environment.
• Work with suppliers in a wide range of Quality relevant areas such as First Articles, general Quality and Regulatory requirements. Work with suppliers on Corrective & Preventative Actions, Root Cause Investigations, conduct Supplier Performance Reviews and reporting of Key Supplier Quality metrics.

Interested applicants should have:
• Proven experience in Medical Devices QMS to develop world-class supply chain processes to suit a low volume, high complexity multi-technology environment.
• Have led projects to manage suppliers to deliver quality product to internal customers, through product & process investigations & evaluations. Identified and driven process improvements with suppliers.
• You will have focussed on and been responsible for supplier process improvements and updating quality system procedures to achieve both fully compliant and lean processes with suppliers.
• Minimum of a Bachelor’s degree in a relevant technical discipline (ideally Quality, Engineering or Science). At least 8 years’ relevant experience in a regulated environment with a core appreciation of FDA regulations and Risk Management including writing and / or reviewing Quality related procedures, plans and reports.

• Strong leadership skills and ability to influence cross-functional teams to drive workscope to completion.