**Overview**:
Validations and Sterility Assurance Technician
**Responsibilities**:
Preparation of protocols and reports for the qualification of equipment, facilities and plant services.
Execution of qualification tests.
Maintenance of the Master Plan for Qualifications and Calibrations.
Preparation of protocols and reports for the validation of manufacturing and cleaning processes.
Supervision of the aseptic process and preparation of the documentation associated with APS.
Qualification of decontamination and sterilization cycles.
Qualification of the visual inspection process.
Validation of GMP computer systems (CSV).
Investigation of deviations. Management of Change Controls and CAPAs.
Updating and reviewing standardized operating procedures.
Maintenance of the GMP archive.
Support in audits and inspections.
**Qualifications**:
Degree in Pharmacy, Chemical Engineering, Biotechnology or similar.
Master in Pharmaceutical Industry.
English level C1 or equivalent.