Computerized Instrument Validation Lead
4 days ago
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana, and our employees work together to discover and bring life-changing medicines to those who need them.
We are seeking a Computerized Instrument Validation Lead to join our team at our Next Generation Biotech Drug Substance Manufacturing Facility in Limerick, Ireland. This individual will be responsible for providing technical oversight for computerised instrument validation (CSV) processes, in accordance with site and corporate procedures and GMP guidelines.
- Develop project plans, prioritize validation activities in line with overall project schedules.
- Manage and coordinate computer system validation deliverables for new and existing projects.
This role requires a Bachelor's Degree in Information Technology, Computer Science, Engineering, or a related field, along with minimum 5+ years of experience in a biotech or pharmaceutical setting.
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