Quality Inspector, Medical Devices - Precision with Global Impact

Edwards Lifesciences Gruppe; Limerick; Presencial; EUR 32.000 - 48.000; Jornada completa

Descripción de la vacante

Edwards Lifesciences in Ireland is seeking a Quality Inspector to visually, dimensionally and functionally inspect medical device components and finished products. You will review documentation, operate inspection equipment, and contribute to compliance with GMP, GDP and SOPs.

You will work in a detail‑oriented team, perform line clearance, participate in audits and training, and support continuous improvement initiatives to ensure products meet design specifications and regulatory requirements.

Formación

• 2 years of previous related experience, including GMP and GDP Required.
• Leaving Certificate or equivalent Preferred.
• Good communication and English reading/writing skills.

Responsabilidades

• Perform visual, dimensional, and functional inspection on a wide variety of components and/or finished medical device products.
• Utilize a microscope in the inspection of equipment and products in line with SOPs.
• Operate automated inspection equipment to verify dimensional requirements and conduct functional testing of complex devices.
• Review, follow and perform job functions in compliance with SOPs and record traceable information in device history records.
• Provide feedback to the team and escalate issues to Engineering Support when needed.
• Perform line clearance and verification of inspection and verify manufacturing documents against drawings.

Conocimientos

Visual inspection

Dimensional inspection

Functional testing

Microscope operation

QMS documentation

Educación

Leaving Certificate or equivalent

Herramientas

Vision inspection system

Automated inspection equipment

Descripción del empleo

Edwards Lifesciences in Ireland is seeking a Quality Inspector to visually, dimensionally and functionally inspect medical device components and finished products. You will review documentation, operate inspection equipment, and contribute to compliance with GMP, GDP and SOPs.

You will work in a detail‑oriented team, perform line clearance, participate in audits and training, and support continuous improvement initiatives to ensure products meet design specifications and regulatory requirements.