Lykke Nyholm Madsen (born in 1962) has a solid experience with the entire value chain in pharmaceutical production and is today acting as consultant for various pharmaceutical companies and the Danish healthcare system. She earned her Master of Science in Pharmacy at The Royal Danish school of Pharmacy in 1989. She is a trained lean leader and has a Certificate in Business Administration from AVT business School Copenhagen.
She has been managing the production of API, production of pharmaceutical products and packaging of finished goods for customers all over the world. Quality assurance and GMP are part of her DNA as she has also been heading QA departments.
She creates cross-organizational results using strong communication and collaboration skills. Her QA background and production experience means that she can act as a facilitator between QA and the production. Her working life has been filled with Change Management tasks, where the art is to implement plans and visions from the top management level, while managing the well-being and development of the employees and promoting their commitment at the same time.
In August 2020 she joined Kyvsgaard Consulting A/S and established the pharmaceutical advisory part of the company. She works with implementation of improvements, ensure anchoring of new processes, internal and external manufacturing, support during change managements processes, recruitment, onboarding and other tasks as well.