The role:
PE Global is currently recruiting for a Quality Systems Specialist on behalf of a leading pharmaceutical company based in Dublin.
This is an initial 12-month contract role.
Overview:
Specialist, QA Systems will join the Document Control Team and, along with other team members, will act as a key point of contact and provide cross-departmental support for a variety of document management systems and processes.
Responsibilities:
Preparation and issuance of controlled documentation to support manufacturing and testing activities
Development and maintenance of the Documentation Management System
Provision of training and user support for the Document Management System
Management of the Document Archive and Record Retention Systems
Maintenance of other document systems and processes e.g. SharePoint, Periodic Review tracking.
Delivery of GMP/GDP training
Participation in the internal and external audit program
Collection of quality metric data
Support completion of investigation/CAPA activities as applicable to role
Interface with relevant departments to ensure compliance with corporate policies, GMP and regulatory requirements
Authoring, review and approval of QA-related procedures
Education and Experience:
The successful candidate will hold a BSc in life sciences/pharmacy or similar
A minimum 1-2 years' Quality experience in a pharmaceutical environment is adventitious
Working knowledge of cGMP requirements for manufacturing and/or systems and compliance.
The candidate must be able to work across a team matrix in order to meet accelerated timelines
The candidate must be able to reprioritise tasks as required to meet changing demands.
Interested candidates should submit an updated CV.
Please call Kellie on ********** or alternatively send an up to date CV to ******
Important note: our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland.
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