Jonna Lindholm
About Jonna Lindholm
Jonna Lindholm is the Senior Manager of GCP Compliance at BeiGene in Basel, Switzerland, with extensive experience in clinical quality management and a strong educational background in chemistry and engineering.
Current Role at BeiGene
Jonna Lindholm serves as a Senior Manager, GCP Compliance at BeiGene in Basel, Basel-Town, Switzerland. In this role since March 2020, she leads the development and implementation of process improvement strategies related to Clinical Compliance in BeiGene's European region. Her responsibilities include ensuring compliance with applicable GCP regulations and adherence to government, industry, and company clinical compliance standards.
Previous Positions in the Pharmaceutical Industry
Jonna Lindholm has extensive experience in various roles within the pharmaceutical industry. She worked as a Clinical Quality Manager at Pharmacyclics, an AbbVie Company, from 2018 to 2020 in Switzerland. Prior to this, she held a GCP Project Manager position at Roche for six months in Basel, Switzerland, from 2017 to 2018. Before joining Roche, she was a GCP Quality Consultant at Eli Lilly and Company, covering the Benelux region from 2016 to 2017 in Brussels, Belgium, and earlier in Finland, Estonia, Latvia, and Lithuania from 2010 to 2015 in Helsinki, Finland.
Early Career and Research Experience
Jonna Lindholm began her career as a Quality Control Associate at Regeneron Pharmaceuticals, Inc. in the Greater New York City Area from 2008 to 2010. She gained research experience as a Research Assistant at Northeastern University / The Barnett Institute of Chemical and Biological Analysis from 2006 to 2008 in Boston, MA, USA. Additionally, she worked at Johnson & Johnson, JSC Janssen Supply Chain as GMP Management; Stability Integrator/Owner for six months in Beerse, Belgium, from 2015 to 2016.
Educational Background
Jonna Lindholm has a strong educational foundation. She holds a Master of Science in Chemistry and Chemical Biology with a specialization in Analytical Chemistry from Northeastern University. Additionally, she earned a Master of Science in Engineering with a focus on Automation and Control Engineering from Tampere University of Technology, and a Bachelor of Science in Engineering in Chemical Engineering from Satakunta University of Applied Sciences. Her academic background has significantly contributed to her expertise in the pharmaceutical and biotech industries.
International Work Experience
Jonna Lindholm's career is marked by international work experience. She has worked in Switzerland, Belgium, Finland, and the USA. This global perspective has equipped her with a deep understanding of regulatory and compliance standards across different regions. Her roles have spanned various functions and responsibilities, showcasing her versatility and commitment to maintaining high standards of clinical compliance and quality in the pharmaceutical industry.