Do you have experience in Cleaning validation and validation of programmes (CSV, data integrity)? Do you have experience working in GMP environments or cleanrooms? Do you have experience supervising or line managing a team?
I am currently working with a brilliant client based in Scotland who specialises in cell and gene therapy. This company's mission is to make Scotland one of the top locations for cell and gene industry. This company helps clients overcome challenges they might face when developing and bringing these therapies to the market and they also have a brand new facility and state of the art labs.
There has been a recent opening for a Validation Supervisor/Manager who's main responsibilities would be equipment validation, cleaning validation and system validation. The right candidate will also line manage the validation team members and ensure that documentation is in line with GMP and SOPs.
The right candidate will have experience in:
Experience in management of GMP validation programmes including CSV and Data Integrity.
Experience in GMP sterile or cleanroom Manufacturing.
Experience in supervising a team.
If you have the relevant experience and would like to hear more about the role then please apply!