Description
As Ireland's Pharmaceutical presence continues to grow, so does our global biopharmaceutical client. With an extensive project portfolio, we are looking for a CSV Engineer to join the team.Located in Munster merely a 15-minute drive from the nearest international airport, Cork cements itself as a hub of pharmaceutical activity. With the historic city of Cork only a stone's throw away, this one of a kind facility is used to host a range of products to treat ultra-rare disease as well as several award winning projects.
As a CSV Engineer, you will be responsible for:
- Investigate process and quality problems and implement corrective actions.
- Follow Biotech/Pharmaceutical industry standards in generating and updating supporting documentation such as P&IDs, material and equipment specifications, requirement and design specifications and validation protocols.
- Work within cross-functional teams.
- CSV experience in sterile product manufacturing and building management would be an advantage (min 3 - 5 years).
- Project Management skills.
- Experience with ISA S95 and S88 standards.
- Experience in the implementation of a risk based validation approach as per ASTM E2500- Preferred but not required.
- Experience with MES Systems - preferred but not required (Werum PasX, Emerson Syncade, etc.).
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