Quality assurance at SK Pharma Logistics
This also includes the preparation and review of qualification documentation. In addition, Ms. Ohlendorf is also responsible for the preparation of process instructions and the implementation of employee training on plant qualification and related GMP topics.
Ms. Ohlendorf previously worked for several years in the pharmaceutical industry in the areas of quality assurance and manufacturing. She has broad experience in all important GMP topics. In particular, she knows the topic of plant qualification from the perspective of both the pharmaceutical customer and the plant supplier.