Supplier Quality Engineer

TC110155
  • €40,000 - 62,000
  • Longford, Republic of Ireland
  • Full Time

About the Company

Our client is a leading global medical device manufacturer with a strong reputation for innovation, quality, and regulatory excellence. Operating from their advanced manufacturing facility in Longford, they partner with many of the world's leading healthcare companies to deliver high-quality medical technologies. Due to continued growth, they are seeking a Supplier Quality Engineer to join their Quality team.

About the Role

As a Supplier Quality Engineer, you will work closely with suppliers to ensure the quality of raw materials and components, helping to deliver high-quality products while maintaining compliance with industry regulations and quality standards. This role offers the opportunity to collaborate with cross-functional teams, drive supplier performance, and support continuous improvement initiatives across the supply chain.

Key Responsibilities

  • Conduct supplier audits and prepare audit reports, ensuring timely follow-up of CAPAs.
  • Investigate and manage supplier quality issues and complaints, including the authority to quarantine or reject non-conforming raw materials.
  • Maintain the Approved Supplier List and supplier quality documentation.
  • Identify critical raw material quality parameters and implement improvement initiatives.
  • Build and maintain strong relationships with key suppliers through regular performance reviews.
  • Support supplier development and continuous improvement activities.
  • Work closely with Manufacturing, Quality, Engineering, and Procurement teams to resolve supplier quality issues.
  • Ensure supplier compliance with quality standards and regulatory requirements.
  • Analyse supplier performance data and identify trends to reduce risk and improve quality.

Requirements

  • Degree in Engineering, Science, Quality, or a related discipline is desirable.
  • Previous experience in Supplier Quality, Quality Engineering, or Manufacturing Quality within a regulated manufacturing environment.
  • Knowledge of ISO 13485 and medical device quality requirements; auditor qualification is advantageous.
  • Experience conducting supplier audits and managing supplier quality performance.
  • Strong analytical and problem-solving skills.
  • Excellent communication and relationship management skills.
  • Strong attention to detail with excellent organisational skills.
  • Comfortable working cross-functionally and engaging with suppliers.
  • Willingness to travel occasionally (up to 25%).

What's on Offer

  • Opportunity to join a leading global medical device manufacturer.
  • Excellent career development opportunities.
  • Competitive salary and benefits package.
  • Collaborative and supportive working environment.
  • Exposure to global suppliers and continuous improvement initiatives.
Tina Cornally Regional Recruitment Manager - Engineering, Manufacturing & HR

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Accessibility 

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Reasonable Accommodations

Our commitment is to make any reasonable accommodation for you in the recruitment process to give you the best opportunity to perform to your optimum in the application, test, and interview process.