• 12 Month Contract
  • Limerick

Systems Co-Ordinator

Industry : Pharmaceutical

Department: QA Compliance & Quality Systems

Essential Duties and Role Responsibilities include, but are not limited to, the following:
 Compliance review of change controls.
 Generation of daily/weekly metrics.
 Compliance review of asset management system records.
 Quarterly reports for partnered products. Generation of metrics for partnered products. Reconciliation of partner notifications/responses.
 Change control team scheduling management – work in progress, incoming and outgoing assignments.
 Organisation/scheduling of change review board. Generation of meeting minutes, and issuance of approval forms.
 External department task management within change control system.
 Hosting/chairing of daily and weekly team meetings.

Education and Experience:
 Requires BS/BA in Life sciences/Engineering or related field. May consider another degree discipline with relevant experience; cGMP experience is desirable.
 2+ years’ experience.
 Relevant experience may be considered in lieu of educational requirement.

Duration:  12 month contract

Location:  Limerick

To apply for this job email your details to enquiries@qaresources.com.