Description
Global pharmaceutical company require a Lead Validation Engineer for their expanding sterile site in Scotland. This is an initial 6-12 months to aid the site in achieving PQ activities later this year.Working on a variety of CAPEX investments throughout 2017 and on ongoing site maintenance projects the Validation lead is required to provide specialist expertise in the areas of: Cleaning Validation, SIP (steam in Place) and autoclave Validation.
The successful candidate will be directly responsible for a small team of client side Validation Engineers and a number of subcontracted companies on a mixture of process and building related projects.
Responsibilities include:
- Approval of Validation.
- Approval of executed works and documentation.
- Approval of executed protocol documentation across the above systems and processes.
- Close supervision and mentorship of Validation execution activities across sterilisation equipment and cleaning processes.
- Day to day management of Validation activities across API sterile projects.