Ivana Panev

• Management and oversight of manufacturing of excipients, drug substance and IMP at Ethris CDMO Network • Management and oversight of QC testing of excipients, drug substance and IMP • Management and oversight of stability studies of excipients, drug substance and IMP • Participation in QMS procedures (OOS/deviation management, CC, supplier qualification, PSF) • Review of regulatory documents

• Preparation of Standard operating procedures and Working instructions for Quality control as a part of QMS • Developing Specifications and Methodologies for the quality examination of raw materials, intermediates and finished products according to a Pharmacopoeia • Quality control analysis • Certificates preparation according to the obtained results • Preparation of Module 3, Section 3.2.P Drug Product as a part of the Common Technical Dossier of pharmaceutical products (CTD files)

Courses – Organic Chemistry, Inorganic Chemistry, Biochemistry • Leading discussion sections, tutorials and laboratory sections • Demonstrating use of laboratory equipment, enforcing laboratory rules • Completing laboratory projects prior to assigning them to students • Evaluating and grading examinations, assignments and record grades • Informing students of the procedures for completing and submitting class work, such as lab reports • Preparing or proctoring examinations

• Dispensing medications and related supplies, according to physicians' prescriptions • Checking for drug interactions • Recommending drug therapy changes when appropriate • Counseling patients regarding appropriate use of medications • Educating patients and staff on drug therapies • Collaborating with other healthcare professionals to plan, monitor, review, and evaluate patient effectiveness • Overseeing daily ordering, as well as automatic refills