Morgan McKinley is partnering with a leading Cork based medical device manufacturer who is seeking a CSV Engineer for an hourly rate long term contract.
The Role;
- Lead the validation of computerized systems, including the development and execution of Validation Plans, IQ/OQ/PQ protocols, and Summary Reports.
- Drive and implement system-related improvements to ensure predictable performance across all product lines, focusing on risk reduction, data integrity, and process automation.
- Provide effective and responsive CSV support to Operations and IT to meet site objectives regarding quality, compliance, and system uptime.
- Lead in-depth investigations into software and system failures using structured problem-solving methodologies to identify and document true root causes.
Required;
- Minimum of bachelors of science degrees in engineering / manufacturing
- 5+ years of experience in a Pharmaceutical or Medical device manufacturing environment (must be GMP regulated).
If you are keen to further develop your career with a leading Medical Device company while working with a highly collaborative team please reach out today to hear more about this exciting opportunity. For more information please contact Orla Casey 021 230 0497
