Senior QA Specialist €29.42 p/h Reporting to the Senior Manager, QA Compliance, the Senior Specialist, QA Compliance will support supplier quality operations for the manufacturing site in Dublin 15.
This is a contract position until 31 Dec 2024.
Key ResponsibilitiesRelease incoming materials for use in manufacturing operationsSupport qualification of new suppliers/materials and requalification of existing.Assess supplier change notifications for impact to qualification status.Support material certification and direct dispense programs.Review and approve quality agreements.Authoring, review and approval of QA-related procedures.QA review, assessment and approval activities for Biologics Manufacture, as applicable, for:Change controlsDeviations/InvestigationsCAPAsOther associated documentationSupport OpEx programs and champion continuous quality improvement initiatives.Qualifications & ExperienceBSc in Science or related discipline with a minimum of 2 years' Supplier Quality or related experience in a Biologics or Pharmaceutical environment.
A clear understanding of cGMP requirements for QA systems and compliance and/or manufacturing.
Detailed knowledge of Biologics Processing would be a distinct advantage.
Required to work on his/her own initiative in addition to working as part of a team.
Excellent communication, presentation, time-management and organizational skills are essential.
Employees are expected to display the BMS Biopharma Behaviours, which enable them to be successful and perform at their highest level.
#J-18808-Ljbffr