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Assoc Quality Engineer

Together, we will change healthcare worldwide.

Join us in our Mission to alleviate pain, restore health and extend life worldwide.

Let's work together to address the universal healthcare needs and improve patients' lives, optimize costs and efficiencies, and expand global access.

Together, we can make a real difference in the global disparity in care.

By providing quality care at the lowest possible cost, we will succeed as a company, and take the future of healthcare Further, Together.

Within the Quality Engineering Validation Department in Medtronic, plc, we focus on execution of process validation activities that exceed the requirements and expectations of patients, physicians, regulatory agencies and the business.

Quality engineering are directly involved in the development of the validation strategies and execution of the validation activities releasing novel processes and products to commercialization.

You will be responsible for the execution of process validation activities for new products, technology transfers and improvement projects.

You will provide Quality input into new product development, process improvements and change control.

You will support the characterization and risk assessment of manufacturing processes and associated equipment.

You will work with project team members to establish process controls that ensure the safety and efficacy of the product.

You will liaise with cross functional team members, to plan and execute on quality engineering deliverables.

You will participate in and support root cause driven approaches to problem solving efforts for quality issues.

You will use and establish analysis techniques and other quality tools to aid decision making.

You will apply the quality system to product development related product builds.

We are looking for a qualified person to Third Level Degree in Science, Engineering or related discipline (Minimum level 7 National Framework of Qualifications or equivalent qualification) and desirably with 1+ years relevant experience.

You are a dynamic team player and can work effectively and proactively on cross-functional teams.

You are experienced with working in the medical device industry or a related environment.

Knowledge and experience in validation would be beneficial.

A good understanding of AGILE (configuration management system), SAP (enterprise resource planning) and TrackWise (Corrective and Preventive Action system) is also desirable.

Solid interpersonal, communication and organizational skills are desirable.

Practical working knowledge of quality improvement tools and techniques would be beneficial.

You are a good communicator and fluent in English, both in writing and speaking.

Leadership Expectations provide the framework for what we expect from all employees at Medtronic - outlining the actions and behaviors we must develop and demonstrate in pursuit of our Mission and global growth goals.

We are co...