Quality Manager

Profile

Job Overview
We are seeking a Quality Manager
for a manufacturing facility in Listowel. The client, a medical device company are a 24/7 production operation and is an ISO 13485 and ISO 9001 accredited company.
The successful candidate will ideally have a qualification in
Engineering
or
Quality
discipline and will have manufacturing experience, with particular emphasis on high-volume low-cost production.
As Quality Manager you will have responsibility for overall management of the QMS. Working in close liaison with the Production Department, you will have ultimate responsibility for the quality of the product.
Key areas of Responsibility:
Gain an in-depth understanding of the products.
Manage product non-conformance (identified either internally or via customer complaints), raising and implementation of CAPA
Investigation, CAPA implementation where applicable and closure of Customer Complaints
Have overall responsibility for entry to and exit from Quarantine (raw materials and finished goods)
Maintain the highest level of product traceability at every stage of the production process and ensure product containment in the case of non-conformity
Liaise with Company Management and the Production, Maintenance, Toolroom and Admin departments
Manage ISO audits and other ISO activities
Manage Customer visits and audits
Manage regulatory requirements and ensure adherence e.g Reach
Identify opportunities for improvement in the QMS
Continually seek to drive quality improvements in both product and process
This is primarily a day shift role, however some presence on other shifts in an ad hoc basis may be required. A minimum of 5 years' experience in a related discipline is a requisite for this position. This is a senior hands-on role and is a full time permanent on-site position
Please apply through the link provided or ****

Company info

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