Senior Quality Engineer (Aortic)., Galway
Client:
Medtronic
Location:
Galway, Ireland
Job Category:
Other
-
EU work permit required:
Yes
Job Reference:
4682a8565612
Job Views:
7
Posted:
24.06.2025
Expiry Date:
08.08.2025
Job Description:
Medtronic
At Medtronic, 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
At our Quality Department in Medtronic, plc, we focus on supporting the product to ensure that customer & patient needs are met every day. Our key focus is on delivering and maintaining a high level of Quality to ensure that business and performance goals are achieved. The Senior Quality Engineer is directly involved 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.
Come for a job, stay for a career!
A Day in The Life Of:
Responsibilities may include the following and other duties may be assigned:
* Develops, modifies, applies and maintains quality standards and protocols for processing materials into partially finished or finished Aortic product with limited supervision.
* Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
* Participates in preparing / critically reviewing/approving NCMRs/ CAPAs/ Investigations and validation activities, providing expert QA technical direction and solutions as appropriate.
* Ensures effective product control measures in the event of issues being noted.
* Provides guidance, coaching, training, delegation of work and review of others' work to other employees within job area.
* Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
* Ensures that corrective measures meet acceptable reliability standards, and that documentation is compliant with requirements.
Key Skills & Experience
* Bachelor’s degree Level 8 in Engineering, Science or technical field with 4+ years of experience in Quality and/or
* Medical Devices OR Advanced degree in Engineering, Science or technical field with 2+ years of experience in Quality and/or Engineering.
* You are technically orientated with a strong risk-based approach to problem solving. You can work independently under limited supervision to determine and develop this best approach.
* You are a dynamic team player and leader and can work effectively and proactively on cross-functional teams with a high level of enthusiasm and motivation.
* Strong communication, organizational, presentation and leadership skills are desirable.
* Experience with Agile, SAP and SAP ME an advantage.
Medtronic offer a competitive salary and flexible Benefits Package
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