Validation system:

Maintains Validation system. Analysis and continuous improvement.
Organization the validation and similar activities, building of temporary multifunctional teams.
Participating in new/alternative materials and combinations testing/validation within multifunctional teams;
Maintains Validation master plan, planning of validation, qualification and similar activities, maintain documentation and data base;
Maintains QMS documentation related to validations, qualification and similar activities;
Performs training in the matter. Maintaining of training documentation;

Control and measurement devices (CMD) system:

Maintains CMD system: QMS documentation related, records, data base. Maintains CMD master calibration plan;
CMD system continuous improvement and efficiency increase;
Work on continuous cost reduction;
Knows the related to a CMD standards;
Knows the related to Medical device standards` requirements concerning CMD and assures their implementing and development;
Maintains the planning and assurance of the CMD system, calibration, distribution;
Monitoring of CMD through the organization – use, condition, need of additional activities;
Organising of all necessary activities for achievement of all planned and required activities;
Performs training to the staff in CMD field as assurance of proper use and relative results. Maintains the training documentation;

Performs tasks required by Director Quality and RA and/or her direct manager upon daily and occasional necessities;