Description
Our biopharmaceutical client requires a Continuing Validation Engineer to join them on an initial 12 month contract.
Key responsibilities
- Experience in Validation specifically continuing (re-validation or maintaining a qualified state in relation to equipment).
- Experience in gap analysis assessments.
- Experienced Technical writer.
- Experience in Deviation/Change control writing.
- Experience in continuing assessments of equipment.
- Capable of managing a large program, therefore project management skills would be necessary.
- An excellent understanding of how manufacturing/Cleaning Validation/HVAC equipment works.
- Equipment includes chromatography skids and bioreactors.
- Cleaning Validation experience would be beneficial