To be involved in the Validation Life Cycle for a Pharmaceutical Manufacturer.
- Experience with Cleaning and Facilities Validation
- Have previously wrote and executed documentation across the full Validation Life Cycle (DQ, IQ, OQ, PQ)
- Have a Pharmaceutical GmP Background.
- Responsibility working on Quality Management, such as CAPA's, non-conformance and deviations.
To find out more about Huxley Engineering, please visit
Huxley Engineering, a trading division of SThree Partnership LLP is acting as an Employment Business in relation to this vacancy | Registered office | 1st Floor, 75 King William Street, London, EC4N 7BE, United Kingdom | Partnership Number | OC387148 England and Wales