Senior Quality Advisor

As QP, Rikke is a valuable advisor and collaborator in GMP and compliance related topics, especially related to drug production, API production, supplier evaluation and validation plans. She is also very experienced in preparation of GMP documentation and overall Quality Management Systems. Experienced in interpretation of External requirements into internal processes.

Rikke has solid experience with daily and project related tasks, also in classified and aseptic production facilities, including Environmental monitoring, Microbiological analysis and Cleaning Validation. Rikke also has a solid experience with API-related activities such as supplier audits and supplier quality agreements and contracts, production, storage and transportation.