• Preparation of documentation for variations, license renewals, and new drug registrations for human and veterinary use.• Reviewing and updating SmPC, PIL, and LL texts according to agency requirements.• Checking drug drafts and packaging before printing.• Preparing documentation for formal deficiencies, clock stops, and other supplements upon the request of the Medicines Agency.• Responsible for the quality of the veterinary drug warehouse according to GDP guidelines and… Show more • Preparation of documentation for variations, license renewals, and new drug registrations for human and veterinary use.• Reviewing and updating SmPC, PIL, and LL texts according to agency requirements.• Checking drug drafts and packaging before printing.• Preparing documentation for formal deficiencies, clock stops, and other supplements upon the request of the Medicines Agency.• Responsible for the quality of the veterinary drug warehouse according to GDP guidelines and deputy responsible for the quality of the human drug warehouse. Show less

• Registering new products – dietary supplements in the Ministry of Health database.• Advertising products on social media.

• • Responsible for drug registration, license renewal, and reporting variations.• Creating text for primary and secondary packaging, PIL, and SmPC.• Communication with ALIMS regarding systematic controls and other activities as needed.• Drug registration for Bosnia and Herzegovina.• Preparing documentation for each batch of drugs produced in the factory with contracted control laboratories, stability studies, etc.• Preparing documentation for the introduction and… Show more • • Responsible for drug registration, license renewal, and reporting variations.• Creating text for primary and secondary packaging, PIL, and SmPC.• Communication with ALIMS regarding systematic controls and other activities as needed.• Drug registration for Bosnia and Herzegovina.• Preparing documentation for each batch of drugs produced in the factory with contracted control laboratories, stability studies, etc.• Preparing documentation for the introduction and recertification of standards: GMP and HACCP.• Developing new products (formulation of tablets, capsules, powders, and gels) for pets, including the entire new product line VetaPro.• Procurement of raw materials, packaging, labels, boxes, and control stamps necessary for production.• Developing a new drug from formulation to registration. Show less

• Working with patients on issuing prescription and non-prescription drugs, cosmetics, and dietary supplements.• Communicating with wholesalers for drug orders and complaints.• Administrative tasks: collecting invoices for drug entry and exit, informing management about adverse drug reactions reported by patients.

• Preparing magistral drugs: powders, liquid and semi-solid preparations for external and internal use, suppositories, and vaginal suppositories, as well as sterile products.• Issuing prescription drugs, OTC drugs, dietary supplements, and cosmetic products.