Lilly is a global healthcare leader headquartered in Indianapolis, Indiana. We give our best effort to our work and put people first.
We are looking for a Specialist QC Esystems who will provide technical support for the electronic systems within the Limerick Quality Control Laboratory (QCL). This role will support the QCL electronic systems project implementation, ensure compliance and operational support of the laboratory electronic systems associated with all testing activities within the QCL function.
Key Responsibilities:
* Serve as a key technical SME on the QCL electronic systems, including LIMS and Empower.
* Provide guidance to the laboratory on the configuration and optimal use of Esystems.
* Configure master data, worksheets, methods, and reports within the QCL electronic systems.
* Support the Authoring/review of key GMP documents such as GMP standard operating procedures, training materials, test methods creation documents, local qualification documents, lab/equipment/computer system periodic reviews, annual product reviews, validation master plans etc.
* Train other team members on core QC Esystems.
* Coordinate across business departments and stakeholders, gathering, and supporting the implementation of enhancement requests for the QCL electronic systems.
Requirements:
* Hons Degree Qualified – B.Sc. in Chemistry, Microbiology, Information Technology or related discipline, with a minimum of 6 years relevant GMP experience.
* Technical expertise in Quality Control applications e.g. Lab Vantage, MODA, Empower, NuGenesis, and benchtop applications such as DataPro2, SoftMax Pro.
* Highly competent in the use of digital solutions for data, equipment, and laboratory management.
The estimated salary for this position is around €60,000 - €80,000 per year, depending on location and experience.