Quality Engineer Validation Audits and CAPA

Westmeath  ‐ Onsite
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Description

Quality Engineer - Medical Devices

My exclusive client is a leading medical device company based in Westmeath and they are urgently seeking an experienced quality systems engineer. This company is expanding due to continued success and it offers great opportunity for progression, an attractive facility and a good atmosphere to work in.

The quality engineer role:
You will be reporting directly to the Quality Systems Manager alongside a team of four
Your role will involve document control, change control systems and internal audits
You will be responsible for providing quality systems support for all processes related to QMS.
You will need to assure that quality standards are maintained and assist with the implementation and compliance of the quality management program.
Part of your role is to support company goals and objectives, policies and procedures, quality systems, and FDA regulations.

Essential for the quality engineer role:
Bachelor's degree in Engineering, Science or related subject.
A minimum of 5 years industry experience.
Medical device experience is essential
Strong experience in at least one of the following is necessary - experience in more than one of these areas is highly advantageous:
Validation experience
Internal Audits
CAPA's

The following is also desirable:
Experience in working in High Volume Production Facility
Strong document management skills
Familiarity with ISO quality systems (ISO9001, ISO14001 and/or ISO13485)

The ideal candidate will be self motivated, be able to hit the ground running and will be a good communicator.

There is an excellent salary of €50,000 - €55,000 plus benefits

If you are interested in this position please contact me Adele Moran on for more information and for immediate consideration.

To find out more about Real please visit www.realstaffing.com
Start date
07/2013
From
Real Staffing
Published at
02.07.2013
Project ID:
559841
Contract type
Permanent
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