Quality Technician

CREGG; Galway; On-site; EUR 42,000 - 52,000; Full time

Job summary

CREGG Recruitment is recruiting a Quality Technician for a leading multinational medical device company in Galway. The role involves plant-wide internal audits, QA documentation, and ensuring GMP compliance while maintaining high attention to detail.

The successful candidate will perform routine testing, review non-conformances, and contribute to continuous improvement with strong interpersonal skills and organisational abilities.

Qualifications

• Experience as a quality technician in a manufacturing environment.
• Experience performing internal audits and non-conformance handling.
• Knowledge of GMP/QA documentation and regulatory standards.

Responsibilities

• Ensure compliance to GMP and regulatory standards.
• Routine final functional testing, product release criteria testing, and recording results.
• Review and update QA documentation.
• Control of non-conforming product.
• Problem solving and continuous improvement investigations.
• Perform internal and plant-wide audits as required.
• Review and update QA documentation.
• Demonstrate good interpersonal and organisational skills.
• Communicate concerns about work process related to safety and environment to the Manager.

Skills

Quality control

Regulatory compliance

GMP

QA documentation

Education

HETAC Level 6 or above in Science/Engineering

Job description

At CREGG Recruitment we are currently recruiting a Quality Technician for a leading multinational medical device company in Galway. Candidates with experience working as a quality technician in a manufacturing environment encouraged to apply today.
For more information about this role please contact Rachel Mc Mahon on 086 0127415/[e-mail]

About the job:

This role will involve carrying out Plant-wide Internal Audits as per relevant schedules; Controlling closed Exception Reports/ Non Conformance Reports, Line Audits and Non Conforming Reports that are generated as well as compiling Yield & Scrap Reports and various documents for Management.

Responsibilities include:

• Ensure compliance to all applicable regulatory standards and current GMP procedures and practices.
• Routine final functional testing, product release criteria testing/inspection and recording of test results.
• Review and update of QA Documentation.
• Control of non-conforming product.
• Problem solving and continuous improvement investigations.
• Perform internal and plant wide audits as required.
• Review and update of QA Documentation.
• Good interpersonal skills and organisational skills.
• Excellent attention to detail.
• Communicates any concerns about work process regarding environmental impact, health or safety issues to their Manager.

Key requirements

• HETAC Level 6 or above in Science or Engineering Discipline.
• Minimum of 2-3 years in a similar role.
• Good interpersonal and organisational skills with attention to detail

For more information:
Call Rachel on 0860127415
email: [e-mail]