Position DetailsResponsible for delivery of quality assurance activities to ensure product is manufactured in accordance with GMP and Regulatory requirements.This key role is an individual contributor role whereby the individual must be a self-starter with professional and academic experience in QA.
This key role involves collaboration with other departments such as Quality Control, Manufacturing, Engineering and Technical Services.
Principle Responsibilities Manage the GxP Document Management system as per site proceduresManage the Training Management system as per site proceduresSupport and/or manage assigned areas of the Quality Management System (QMS) including Deviation, Change Control and CAPA management systems; Internal/External audits; Customer Complaints; Vendor Management; review /approval Manufacturing Batch Records and assessment /approval and release of production materials.Generate, review, and approve SOP's/other documentation as applicable to your area of responsibility to ensure compliance with GMP and regulatory requirements.Manage the reference and retention sample programQC Support including review and approval of QC testing documentationIssuance and retrieval of batch records and protocols, logbooksReview and approval of Batch Processing RecordsReview and approval of validation protocols/ reports and related documentation to ensure compliance with current EU regulatory expectations and site procedures.Support QA activities in project work-streams involving cross-functional, multidepartment teams including Operations, Quality Control, Quality Assurance, Engineering, and othersSupport audits and inspectionsActively contribute to continuous improvement activities.Other duties as assigned Education /Experience Third level qualification in a Biological /Pharmaceutical science discipline with a minimum of 3 years' experience working in a in a GMP Quality Environment