Job Title

Quality Assurance Engineer Tullamore


The Role

  • Quality Assurance Engineer (QA)
  • Tullamore
  • Onsite / Remote Hybrid
  • Permanent or Contractor opportunity

Role Brief

The successful candidate will be responsible for a number of Quality responsibilities that support the wider validation function.

Key Responsibilities:

  • Validation support
  • Review of DHF’s & Risk Management Files
  • GAP analysis ability
  • Manage generation of data to support IFU claims

Skills Brief

  • Experience within a quality focused role in a Medical Devices or related regulated environment.
  • Experience in regulatory and industry standards for GMP and GDP.
  • Excellent technical writing skills including deviation reports and validation reports.
  • EUMDR/Medical device experience would be highly advantageous.

Person Brief

Candidates must have a relevant science or engineering tertiary qualification with a minimum of 2 years’ experience in the Medical Devices sector or another closely related regulated environment.

The ideal candidate will have excellent collaboration and communication skills, with a demonstrated understanding of quality processes and related validation and compliance standards. In addition to this, strong attention to detail and an excellent understanding of validation concepts and documentation is required.

The candidate should be based within a reasonable commute of the site location as the role will be mostly onsite with limited remote working if appropriate and in line with project requirements.

Opportunity Brief

This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry leading technology solutions. SL Controls offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation and benefits package, which rewards high performers.

Company Brief

SL Controls are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets.

Over the past 19 years we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway, Limerick, Leinster and Florida USA.

We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM’s and Technology providers.

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