Quality Technician

1 month ago


Dublin, Dublin City, Ireland Cpl Full time

On behalf of our client, we currently have an excellent opportunity for a Quality Technician to join a growing Medical Technology company. Dublin location, predominately site based with some hybrid.

The Quality Technician will work closely with colleagues to support the following activities:

· Creation, review, and approval of QMS documentation.

· Process and product development activities (including validations).

· Execute troubleshooting and investigation activities.

· Assist in analysis of returned product.

· Support operational, facilities and equipment management activities.

· Assist in incoming inspection process.

Responsibilities and Essential Functions:

· Work cross functionally with customer support teams to ensure timely and accurate documentation of customer complaints.

· Assist in investigation of customer complaints and the analysis of returned product.

· Analyse data to identify trends in product quality or defects with the goal of mitigating and preventing recurrence and future defects.

· Identify opportunities to enhance the effectiveness of the quality system and product quality.

· Participate in operational excellence and continuous improvement initiatives using recognised methodologies such as Six Sigma, Lean, Kaizen etc.

· Assist in the maintenance of QMS performance KPIs and preparation of associated reports.

· Assist in the development and maintenance of document control and record management processes.

· Assist in the assignment of QMS training requirements and maintenance of related records.

· Lead spreadsheet validation activities.

· Assist in product related validation and verification activities, as needed.

· Support the execution of the internal audit process and 3rd party audits.

· Any other reasonable duties as required.

Qualifications and Experience:

· Third level Engineering/Manufacturing/Science degree qualification or equivalent.

· 1+ years in regulated work environment (preferably in Medical Devices).

· Internal/Lead Auditor training preferable.

Key Skills

· A self-starter in terms of time and task management and operate with minimal supervision.

· Strong problem-solving ability.

· Good communicator both verbally and in writing with ability to influence.

· Ability to meet deadlines.

· Good understanding of ISO 13485 and FDA QSR quality standards.

· Proficiency in use of desktop software applications such as MS Office.

For full details contact Linda at or email your CV to Thornshaw Scientific is a division of the CPL Group


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