Job Title: Quality Engineer
Location: Celestica Galway, Ireland
A career at Celestica is about making a meaningful purpose with our customers. We imagine, develop and deliver a better future with them.
About the Role:
* Deliver a fully automated high volume manufacturing line from development stage to full scale production ramp producing world class medical devices.
* Responsible for dealing with the three major phases of Quality Management: Quality Planning/Prevention & Corrective Action.
Responsibilities:
* Lead validation activities, process/procedure definition and maintain a continuous flow of high quality products to our customers in a medical device environment.
* Provide expert QE technical direction/input to qualification and validation activities in conjunction with Design, Engineering and extended QA teams.
* Author and support qualification/validation protocols/reports.
* Take effective actions on time in case of quality excursions.
Requirements:
* Strong knowledge of quality tools, QSR, ISO / MDR standards and processes.
* Thorough working knowledge of Risk Management and Validation techniques.
* Knowledge of statistical requirements and software validation requirements is an advantage.
What We Offer:
* Market-competitive total reward: flexible salary, fix and variable salary based on goals.
* The opportunity to become a key member of the new product introduction team in the Health Tech.
* Quality function driven by innovation where creativity matters.