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Manufacturing Engineer

Medtronic


Location:
Galway
Date:
15-12-2017
2017-12-152018-01-14
Job Code:
26704
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  • Engineering Jobs
Medtronic
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Job Details

Company Medtronic
Job Title Manufacturing Engineer
JobId 26704
Location: Galway, IRL

Description
Manufacturing Engineer

Location:

Galway, County Galway, Ireland

Requisition #:

16000BXN

Post Date:

Aug 03, 2017

FURTHER, TOGETHER

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.

OUR PURPOSE

As a Manufacturing Engineer you will be responsible for the Technical and Quality evaluation of vendors processes for the supply of components to Medtronic, Mervue Galway. In addition you will be responsible for ongoing Vendor management to ensure that all sourced parts conform to specification on an ongoing basis.

OUR OFFER

As a Manufacturing Engineer, you will provide technical support to production, materials and manufacturing communicating and resolving any quality issues occurring on a component supplied by this vendor. You will carry out Vendor approval / surveillance audits to ensure that suppliers are capable of meeting Medtronic’s quality requirements on a continuous basis. You will represent the Vendor Engineering group in Design Implementations and Vendor Transfers by generating and executing clear, concise Vendor Process Qualification protocols and reports. You will ensure that “First Articles” are carried out to verify that all parts meet their dimensional and functional requirements. You will manage vendors on an ongoing basis via regular, periodic audits and Quality Improvement Teams to guarantee consistent high quality performance on an ongoing basis. You will participate in cross functional teams to review process improvements / optimizations at suppliers through PFMEA’s and control plans.

YOUR PROFILE

We are looking for a qualified person to
Third Level Degree (BSc) (L8) with at least 3 years in Mechanical, Electronic
or Manufacturing engineering discipline.
You are a dynamic team player and can work effectively and proactively
on cross-functional teams. You are
experienced with process/product development and knowledge of process
qualification and validation techniques. Broad knowledge of materials and
processes applicable to medical device industry is desirable. Experience of
medical device industry regulations (Lead Auditor Certification), manufacturing
engineering role and ability to manage self and others to achieve challenging
targets is advantageous.

SHAPE

We are committed to being experts in what we do, with a clear vision of where we are going and the plan to get there.

■ Demonstrates Global Business Acumen

■ Thinks Critically and Makes Sound Decisions

■ Sets Strategic Direction

ENGAGE

We partner with and involve others, knowing that diverse talent, skills, and perspectives lead to better outcomes.

■ Collaborates and Creates Alignment

■ Attracts, Deploys, and Develops Talent

■ Fosters Diversity and Inclusion

INNOVATE

We are bold thinkers who create new ideas and bring our best solutions forward to benefit our patients, partners, and customers.

■ Focuses on Patient and Customer

■ Generates Breakthrough Ideas

■ Initiates and Leads Change

ACHIEVE

We do what we say we are going to do, delivering results with the highest standards.

■ Sets High Standards

■ Instils Operational Excellence

■ Drives Accountability

■ Models Ethical Behavior

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