We are delighted to be supporting our Galway based medical device client as they expand their Quality team. They are looking to hire an experienced QA Technician which will be based fully onsite supporting production. This role will best suit someone who likes a diverse role and who can work autonomously.
The QA Technician provides quality support to manufacturing operations, ensuring compliance with regulatory standards and internal procedures. The role involves auditing, documentation, non-conformance management, and supporting process improvements within a regulated medical device environment.
Key Responsibilities
- Provide day-to-day quality support to production.
- Conduct in-process, incoming, and 5S audits.
- Manage non-conforming materials and corrective actions.
- Maintain and update Quality Management System (QMS) documentation.
- Support GMP and GDP compliance.
- Prepare and report quality metrics.
- Support validation, product transfer, and audit activities.
- Contribute to continuous improvement initiatives using Lean and Six Sigma tools.
Qualifications and Experience
- Third-level qualification in a quality or related discipline.
- 2–5 years’ experience in a Quality or Operations role within the Medical Device or Pharmaceutical industry.
- Knowledge of ISO 13485, EU MDR, and FDA 21 CFR Part 820.
- Experience in documentation control and auditing.
- Proficiency in Microsoft Office.
- Strong communication, organisation, and problem-solving skills.
For more information and a confidential discussion on the role please contact Amy Newell.
amy.newell@collinsmcnicholas.ie
091 706718