Quality Engineer I

  • Cork
  • Temporary 12 months
  • JO-1907-64609_1562072570

Summary

Responsibilities:

  • Responsible for all operational quality aspects associated with product manufacture and release.
  • Management of complaints systems, tracking, issuing of reports, ensuring effective corrective and preventative actions and timely close out.
  • Investigate Quality problems associated with the production department and implement effective corrective and preventive measures
  • Ensures key quality metrics (CAPA management, First Pass Quality, Complaints, etc) are attained.
  • Drive/support & implement continuous improvement projects with the operations team using Process Excellence lean/six sigma tools.
  • Ensures the pertinent corporate quality and regulatory standards are attained.
  • Maintains strong communication with internal and external stakeholders.
  • Participates / supports the Internal and External Audit Programme.
  • Ensure accurate and effective quality system documentation and reports.
  • Handling customer queries and issues.

Requirements:

  • A degree in an appropriate science/engineering discipline and at least 3 years relevant experience. Preferably in a regulated Medical Device or GMP manufacturing site.
  • Excellent communication skills.
  • Good leadership and planning skills.
  • Technical ability and a good approach to problem solving.

Fastnet has a strict confidentiality policy - please be assured that your details will never be forwarded to any third party without your consent.

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