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Job ID: JOB-13290
QA Engineer – 12 Month FTC

Purpose

The purpose of the position is to provide Quality Engineering services for the site. Develop and implement Master Validation Plans, Risk Assessments and lead QE activities in the Value Stream

Responsibilities

• Develop Master Validation Plans
• Develop and complete DV/IQ/OQ/PQ protocols
• Contribute to the development of FAT/SAT protocols
• Execute Validation Protocols, root cause deviations and generate validation reports
• Develop product specifications / drawings / quality plans in conjunction with NPD personnel
• Provide QE support for New Product Development (NPD) projects
• Process Risk Management / FMEA
• Complete internal audits per the audit schedule
• Co-ordinate and implement process capability analysis on catheter processes
• Complete CAPA investigations
• Lead Hollister Production System (HPS) audits for the department

Experience

• Degree in Engineering/Science Discipline and Quality Engineering Qualification
• Experience in statistical analysis / SPC / validation of automated equipment
• 5 years’ experience in Medical Device Industry utilizing automated equipment
• Master’s degree in Engineering/Science Discipline an advantage

For further information on this role in Mayo please contact Aisling Kidney on 0872197421 or careers@hero.ie

Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/

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Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review you data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

Aisling Kidney

JOB-13290

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