Precision QA Inspector – Medical Devices

Edwards; Limerick; Híbrido; EUR 32.000 - 46.000; Jornada completa

Descripción de la vacante

Edwards Lifesciences in Ireland is seeking a Quality Inspector to assess in‑process and finished medical devices, review documentation, and conduct audits to ensure compliance with regulatory standards and product design specifications.

You will perform visual, dimensional, and functional inspections using microscopes and inspection systems, support line clearance, ensure traceability in device history records, and help train other inspectors in a fast-paced clean‑room manufacturing environment.

Formación

• Must have good communication and written English.
• Strong attention to detail and accuracy in documentation.
• Familiar with GMP/GDP and clean-room manufacturing.
• Able to read and follow SOPs and job instructions.
• Capable of using inspection equipment (microscopes, vision systems).
• Experience in supporting line clearance and traceability records.

Responsabilidades

• Perform visual, dimensional, and functional inspection of components and finished devices.
• Conduct audits and review accompanying documentation for compliance.
• Record traceable information in device history records and QMS.
• Support training of other inspectors and participate in TMVs or first article inspections.
• Ensure timely shift handovers and maintain clean work area.

Conocimientos

Good communication

English proficiency

Attention to detail

Reading comprehension

Teamwork

Feedback negotiation

Safety compliance

Documentation accuracy

Problem solving

Educación

Leaving Certificate

Herramientas

Microscope

Vision inspection system

Inspection tools

Descripción del empleo

Edwards Lifesciences in Ireland is seeking a Quality Inspector to assess in‑process and finished medical devices, review documentation, and conduct audits to ensure compliance with regulatory standards and product design specifications.

You will perform visual, dimensional, and functional inspections using microscopes and inspection systems, support line clearance, ensure traceability in device history records, and help train other inspectors in a fast-paced clean‑room manufacturing environment.