Industry : Pharmaceutical

Department: QA Compliance and Quality Systems

Role Overview:

Essential Duties and 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.

Contract Duration: 12 months

Location: Limerick

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