Description
Our pharmaceutical client, based in greater London area, is looking for a Validation Specialist to prepare and execute validation protocols and reports for a range of production, laboratory equipment, facilities and utilities including controlled storage environments.Knowledge required:
- cGMP in Bio/pharmaceuticals.
- Validation Life Cycle.
- Risk based Approach to Validation and Compliance.
- Quality systems within Bio/pharmaceuticals - CAPA, Change Control, Deviation, Non-conformance.
- Computer system validation desirable.
- Pharmaceutical equipment and systems.
Skills needed:
- Equipment validation and qualification – delivering all aspects of validation lifecycle.
- Use of temperature logging equipment, pref. Kaye Validator 2000.
- Writing and executing validation protocols, setting criteria, test methods, objectives and strategies and preparing validation reports.
Feel free to contact me for more information.