We’re currently recruiting for an exciting opportunity with an award winning pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
• Own and manage Change Controls through their life cycle for QC.
•Lead, contribute to, oversee, run and participate in Root Cause Analysis, implementing improvements and Corrective Actions.
•Trend analysis of Deviations relating to QC.
•Develop and maintain quality systems within QC to ensure ongoing compliance with cGLP.
Education & Experience
• Hold a third level qualification in a Science related discipline.
•Minimum 4 years’ experience in a Biotechnology/ Pharmaceutical/ GMP Environment.
•Knowledge of lab operations, analytical lab techniques, commercialization, and cGMP.
•Experience with Deviations and Laboratory investigations including CAPA identification and implementation.
•Experience in leading Root Cause Analysis would be advantageous.
•Experience in managing and owning Change Controls would be advantageous.
If you would like further Information you can contact the recruiter directly:
Jack Caffrey | Tel: +353 (0) 1 507 9279