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Senior quality engineer

Galway
Medtronic Vascular Galway Uc
Quality engineer
Posted: 11 May
Offer description

At Medtronic, you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

We value what makes you unique. Be part of a company that thinks differently to solve problems, make progress and deliver meaningful innovations. Our Purpose


Our Quality Department

Supports the product value stream to ensure that customer and patient needs are met every day. We focus on delivering and maintaining a high level of Quality to ensure that business and performance goals are achieved.


The Senior Quality Engineer Role

Is critical in supporting key department metrics thus contributing to the global strategy and to deliver on our mission to contribute to human welfare by supporting the manufacture of products that alleviate pain, restore health, and extend life.

In our Structural Heart Post Market Quality Department, we focus on partnering with internal and external colleagues to plan and execute Post Market Strategies for continuous improvement of products, methodologies, processes, and departmental interfaces, while working within the organisation to build, motivate and lead high performance teams.


A Day in the Life Of

Apply knowledge of design control principles and quality engineering techniques throughout the product development process and the product lifecycle.

* Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
* Collaborates with complaints team for complex investigations.
* Provide Design Assurance support to various OU Sustaining & product Surveillance initiatives.
* Review and approve changes to designs and development processes and assess their impact in order to ensure reliability requirements are met.
* Provide input to design and manufacturing deliverables including material specifications, drawings, inspection procedures, and manufacturing procedures, to ensure that the resulting products can be adequately manufactured and tested.


Key Skills & Experience

Requires advanced knowledge of job area combining breadth and depth, typically obtained through advanced education combined with experience. Requires a minimum Level 8 degree in Engineering or other relevant discipline with minimum 4 years' relevant experience.

* May have practical knowledge of project management.
* Experience in a highly regulated industry, preferably medical devices.
* Experience with solving complex issues by interacting with cross functional groups.
* Proven ability to operate in a matrix organization and navigate complex business systems, regulations, standards, and performance requirements.
* Knowledge of reliability tools and practices that effectively support requirements, design, integration and verification, and validation.

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