Dear Job Seekers
Sorry! We didn’t find any related jobs matching your criteria.
This role will involve:
Modify, review, and create Validation Documents, Quality Plans, Specifications, Test Specifications, Validation Reports
Carry out Assessments of computerised systems to ensure that specifications and current regulations are met.
Keep abreast of current Computer Validation related regulations
Carry out system testing against specifications, record test results and review test results in line with current validation regulations.
Work within the regulations required for pharmaceutical projects and manufacturing, e.g., GMP, GAMP
To be successful in this role, you will:
have working knowledge in Validation in one or more of the following areas (Computer System/Process/Project/Equipment/Cleaning etc.) within the Biotech/Med Device/ Pharmaceutical (FDA/MHRA regulated industries).
Typical regulatory knowledge would be in: -