Key Responsibilities:
* Manage lab equipment validation projects from software installation to business release
* Prioritise CSV activities in line with project schedules and monitor budgets
* Generate computer system validation documentation, e.g. Design Spec, Configuration Spec, Testing, Security Plan, Test Summary Report, in accordance with site procedures and GMP guidelines
To excel in this role, you will need a minimum of 3 years of experience supporting and validating lab equipment, updating documentation, system testing, troubleshooting.
You should also have experience analysing and challenging s/w to identify gaps and knowledge of 21 CFR Part 11 requirements, ER/ES and data integrity guidelines.
In addition, excellent oral and written communication skills are required, with the proven ability to communicate and build relationships cross-functionally.
Benefits include an attractive salary and benefits package.