Description
A global Biopharmaceutical leader is currently looking for an experienced CSV Engineer to join their team on a new build project based in Ireland.The responsibilities of the CSV Engineer will include:
- 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.
- Communicate progress effectively.
- Implementation of CSV related Corporate Policies and Procedures. Ensure process and project documentation is accurate and updated.
- Adherence to the Company QMS.
- Commissioning, qualification and validation experience in vaccine or sterile product manufacturing and building management would be an advantage (min 3 - 5 years)
- Strong technical writing and communication skills.
- Ability to close items to completion.
- Ability to work with a high level of detail and to a high standard.
- Problem solving skills.
- Project Management skills