Preparation of the dossiers for the submissions in CTD format of the medicinal products according to the national legislation; Checking and preparing the submission dossiers for promotional materials for OTC products in accordance with the existing information from SmPC, current legislation; Checking and approval of draft design for boxes, foils, and leaflets; Preparing and submission of the documents for variations, quality / DLs, reauthorizations; Preparing the variation and post-approval change packages and other necessary documents as required by the variation process; Maintaining the updated database; Collaborate with the other departments and external partners to successfully deliver the agreed project scope in compliance with the agreed project plans and procedures.

Qualitative and quantitative analytical tests, in compliance with the good laboratory practice standards, procedures, instructions and quality specifications in force; Analysis of methods: HPLC, TLC, UV / VIS, KF, Dissolution, Potentiometry; Validation methods; Maintenance of laboratory equipment.

Physico-chemical analyzes - drinking water;Preparation of the necessary solutions; Filling in daily and monthly reports; Single point of contact - operators department - water treatment station.

Production process - Glass industry

Production process - Cement industry