My Midlands based client has a vacancy for an experienced Quality Engineer:
The Quality Engineer will be responsible for implementing best practice initiatives to improve process capability, and will provide ongoing leadership.
The ongoing drive to improve overall site quality performance by use of root cause analysis tools and techniques
Execution of assigned projects within cost and schedule requirements.
Manage corrective actions to assure effective corrective and preventative actions, to avoid repeat issues.
Supervision of QA operators.
Develop reporting methodologies for Cpk, Ppk metrics for the top product codes at the plant.
Lead training capability development within QA department
Conduct product training
Conduct internal audits and support site during internal and external audits.
Identify and take part in continuous improvements opportunities
A degree in Engineering / Technical discipline or equivalent experience.
A minimum of 5 years experience working in the medical device industry.
Experience working in a quality engineering role with active involvement with the manufacturing floor.
A Six-Sigma certification is desirable but not essential
SKILLS & COMPETENCIES REQUIRED
Experience of working within a regulated industry with knowledge of MDD (Medical Device Directive), ISO 13485 (Quality Management Systems), FDA, cGMP, and Risk Management (ISO 14971)
Experience in a supervisory or leadership role with people management responsibility
Experience working with moulding and extrusion processes and with automated assembly processes is desirable.
Salary dependent on experience
To take advantage of this opportunity call Tanya on (090)6493882 or send your cv
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