Description
One of our key Pharmaceutical Clients requires a CSV generalist to review the pre and post testing validation documentation from a Quality/QA perspective.Duration: Initially 6 months
Location: UK
Our Client has a number of projects currently taking place across site. One is a new Environmental Monitoring System project. This project is in need of an additional person to come in and review and approve the CSV documentation for the project.
Skills and experience needed:
- A strong CSV background.
- Pharmaceutical experience - ideally from a secondary background.
- Experience of reviewing and approving validation documentation, ideally from a QA perspective.
- Extensive years of experience: 10 plus years.
- Good written and communication skills.
- Able to interact with others at all levels.
This is a great opportunity for an Engineer to join a Global Pharmaceutical company in a CSV position.
Please apply now for more information!
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