with MedPharm’s QMS. Performing and planning pre-defined experiments according to internal standard operating procedures (SOP) (e.g... laboratory environment To conduct yourself in concordance with the MedPharm Ethos, professionalism and confidentiality...
) manufacturing and associated Quality Management Systems at MedPharm. The role is responsible for supporting compliance with Good...
Position Summary The Computer System Validation (CSV) Specialist is responsible for the governance, validation, and lifecycle management of all GxP-relevant computerised systems at site. This role ensures ongoing compliance with EU GMP An...