Ingrid Sjöberg has more than 30 years of experience in quality assurance in the pharmaceutical and medical device industry, including from AstraZeneca in Sweden and Ferring Pharmaceuticals in Denmark.
Today, Ingrid runs an independent consulting business, Ingrid Sjöberg Quality Assurance AB, which offers support and advice to larger and smaller companies with operations in research and development of pharmaceuticals and related products. Ingrid has extensive experience in current regulations such as Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Good Clinical Practice (GCP) and ISO standards and has significant experience of working with various authorities.
Ingrid has a broad network within industry and industry associations and has for many years sat on the board of SARQA (the Swedish QA association) and sits as a representative in the OECD Discussion Group on GLP.
Ingrid has a Master of Science in Chemical Engineering from Lund University.
