Nadin Stramka has been working in the pharmaceutical industry since 2011. From 2011 to 2020, she held various positions, initially as a Quality Manager and later as Head of Quality Assurance. Ms. Stramka conducted numerous audits in various GxP areas and was responsible for the development and further improvement of GMP/GCP/GDP-QM-systems.

Since 2020, she has been part of Paar Pharma Consulting and supports our clients on various topics, taking on interim or permanent responsible roles such as leading QM/QA, acting as the responsible person for pharmaceutical wholesale, or as the person for controlled substances(BtM-V).

Her areas of expertise are in the establishment and review of QM systems, creation and verification of SOPs, audit preparation and follow-up, development of training content, and conducting training sessions.

Additionally, she has comprehensive expertise in the areas of manufacturing and testing of medicinal products, wholesale, active substance trading, and narcotics (cannabis).