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Senior manufacturing engineering specialist

Limerick
Cook Medical
Manufacturing
Posted: 26 September
Offer description

Overview The Senior Manufacturing Engineering Specialist is responsible for the preventative maintenance schedule of equipment used in production and engineering.

This person is also seen as a subject matter expert for equipment issue resolution and equipment performance improvement.

Position: Senior Manufacturing Engineering Specialist Department: Manufacturing Engineering Reporting to: Manager, Manufacturing Engineering Responsibilities Maintain and implement the daily and weekly preventative maintenance (PM) schedule for all production equipment and ensure PM documentation and database is completed compliantly and in a timely manner.

Carry out set-up of manufacturing equipment within the production environment.

Record and verify inputs.

Work with equipment manager on the set-up of new equipment task plans / material lists.

Delegates, trains and mentors junior team members in maintenance and engineering activities within the MBU.

Lead on the identification and implementation of process improvements within the manufacturing processes.

Support with the equipment installation process through Infor EAM.

Lead on the resolution of significant equipment breakdowns in production areas and record in Infor EAM.

Review maintenance schedules and task plans on an ongoing basis and propose improvements to same.

Deliver process improvements / continuous improvement activities as required.

Ability and willingness to interact with various functions to problem solve and address equipment/maintenance issues.

Interact with auditors and be seen as a Site Lead in the Maintenance field during audits and inspections.

Ensure that Cook's Code of Conduct is considered in all business matters carried out on Cook's behalf.

Qualifications Minimum of 7 years' experience in a production/technical support role is required.

Production/Technical qualification (Level 7) is preferred.

Proficient in A3 / DMAIC methodology.

Good communication and inter-personal skills.

Proficient in Project Management.

Knowledge of medical device quality standards/practises or similar regulated industry would be an advantage.

Willingness to seek out and drive improvement.

Demonstrated problem solving skills.

Highly motivated individual, self-starter with a passion for excellence.

Good computer skills including knowledge of Microsoft Office.

Proficient in CAD software CREO or similar programs is advantageous.

Must be a good team player who is capable of working well to tight deadlines.

High degree of self-motivation.

Willingness and availability to travel on company business To be considered for this role you will be redirected to and must complete the application process on our careers page.

To start the process click the Continue to Application or Login/Register to apply button below.

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