​What you need to know: 

A leading medical device company that has a global reach and is at the forefront of developing new medical technologies is currently seeking a dynamic and results-orientated Quality Engineer for a 12-month contract in Galway city.

As a Quality Engineer you will be involved in the development and implementation of quality standards and protocol for processing materials and products. You will report directly to the Quality Manager and work closely with the engineering and manufacturing departments to ensure quality standards are met.

This is a 12-month contract. 

Your new job

Key duties & responsibilities include:

·         Develops, modifies, applies, and maintains quality standards and protocol for processing materials into partially finished or finished materials products.

·         Collaborates with engineering and manufacturing functions to ensure quality standards are in place.

·         Devises and implements methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products.

·         Design inspection and testing mechanisms for equipment.

·         Ensure that corrective measures meet acceptable reliability standards, and that documentation is compliant with requirements.

·         Collaborate with project teams and cross-functional groups to develop and deliver quality products.

·         Support Test method validation execution for all internal Test Methods.

·         Evaluate changes being made to material specifications to determine if the method is clear and concise.

·         Support associated validation activities such as IQ, OQ, and software validation.      

What are we looking for?

·         A minimum of a Bachelor’s degree (Level 8 NFQ) in a relevant technical discipline (e.g. Engineering or Science)

·         A minimum of 2 years relevant experience in the medical device industry.

·         A dynamic team player, who can work effectively and proactively on cross-functional teams.

·         Strong organisation and project management skills with the ability to prioritise tasks and meet deadlines.

·         Strong communicator (oral and written) who communicates their ideas concisely and is carrying out presentations.

·         Knowledge of regulatory requirements and guidelines including 21 CFR part 820, MDR, and ISO 13485 requirements.

·         Knowledge of statistical requirements.

Apply for this job now with a Word version of your CV or get in touch with Oliver at oliver@matrixrecruitment.ie

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