Senior Quality Engineer

Location: Galway, Republic of Ireland Salary:
Sector: Quality Assurance (QA) Type: Permanent

Why apply for Senior Quality Engineer?

I am working with my client, a growing medical device company in Galway who require x2 Senior Quality Engineers to join their team. There are positions open in Operations and in NPI - New Product Introduction.

The company are well-recognised in their field and are located in the heart of Galway. This is a full-time, permanent position. You will be compensated with a competitive salary (DOE) plus bonus, healthcare and pension contribution too.

This is a fantastic opportunity for a Quality Engineer who possesses strong supervisory skills and has the ability to lead the quality team with enthusiasm and initiative. Reporting to the Quality Manager of your area, you will be working in an organisation with opportunities to use your quality skillset, through quality improvement projects, across the board.

What will I be doing as Senior Quality Engineer?

As Senior Quality Engineer, you will be a leader in driving quality across your team within the company. Your key responsibilities will include:

  • Investigating the root cause of quality issues and CAPA's to prevent re occurrence
  • Engaging in quality & compliance awareness for GMP standards
  • Preparing quality reports for meetings and management reviews.
  • Quality review of validation documentation.
  • Performing and supporting internal and external audits to ISO and FDA requirements
  • Supporting Operations area projects and initiatives i.e. Kaizen, CFPS etc.

Are you someone who can further develop the QMS and continuously improve it? Can you direct and guide quality engineers and ensure that company expectations and regulatory requirements are met? If so, this challenging and rewarding position could be the one for you.

What do I need to apply for Senior Quality Engineer?

You will need a Bachelor's degree in a scientific/engineering/technical discipline. You are required to have at least 5 years' experience in a medical device manufacturing environment, with a proven track record in Quality Assurance. You need strong knowledge of regulatory environment and have a proven track record of resolving complex quality issues e.g. with CAPA's and root cause analysis. Supervision of quality staff is a distinct advantage.

Meet the above requirements? Think this is the job for you in Galway? Apply today for immediate consideration.

EU passport/Stamp 4 Visa required.

To find out more about Real please visit

Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales