What you need to know
My client in the medical device industry is looking to recruit a Quality Engineer for their facility in Westport, Co. Mayo
This is a permanent job with company benefits.
Your new job
Key duties & responsibilities:
Responsible for oversight of products and releases
Execute product releases including management of customer communication and non-conformance investigations
Participate in corrective actions and continuous improvement activities.
Perform internal audits, remediation and report generation
Create new quality system policies and procedures
Perform statistical analysis and process quality improvement changes.
Monitor and report performance metrics
Lead quality system programs i.e. calibration, maintenance, CAPA, complaints etc
Perform other duties as assigned by the Quality Manager
What are we looking for?
3rd level qualification in Engineering/Quality or related discipline
At least 3-4 years work experience as a Quality Engineer/Quality Systems experience
Experience working in ISO certified environment
Experience of FDA/QSR/EUGMP preferred
Ability to work independently and alongside cross-functional teams
Experience in delegating and leading a team
Excellent management/coordination skills
Strong analytical thinking, problem-solving and decision making
Strong communication and interpersonal skills.
Apply for this job now or get in touch with Lisa Egan on 087-4056165
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