Overview
We are working on an exciting Quality Engineer role for a large medical device client in Clonmel.
Note: no sponsorship is provided for this contract position, a valid working visa is required.
Responsibilities
Navigating Manufacturing Instructions, Procedures and Validations to determine repetitive actions, creation of product disposition instructions and qualification reports.
Assessing site documents for gaps in relation to global documents.
Manufacturing document redlines and updates.
Maintaining listings of equipment and navigating procedures and validation documents to determine equipment documentation requirements.
Qualifications
A Level 8 Degree or equivalent in an Engineering or Science related discipline.
A minimum of 2-3 years' experience working at Engineering level, ideally within the Medical Device industry.
Seniority level
Associate
Employment type
Contract
Job function
Manufacturing and Engineering
Industries
Medical Equipment Manufacturing and Manufacturing
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