In this role you will assist the team in the preparation of validation related documentation, standard operating procedures, reports, system quality reviews, identifying deficiencies, preparing CACI documents, test scripts and change controls with regards to automated systems validation.

Requirements

• Hold a relevant degree in computer science, computer engineering or any other pertinent degree
• Have a minimum of 5 years relevant experience in pharmaceutical industry with in-depth knowledge of FDA and European compliance regulations and GAMP guidelines