Winta Woldai
Bart Croonenborghs
Bart Croonenborghs is a PhD in nuclear and solid state physics, from Leuven University in Belgium. He joined Sterigenics International in 2005 and currently serves as Technical Director Irradiation. Throughout his career with Sterigenics, Dr. Croonenborghs has performed IQ/OQ validation of gamma and electron beam irradiators; designed and executed Process Definition programs (establishing of sterilization […]
Anette Sjögren
Anette has over 30 years of experience from medical device and pharma industry as QA, RA, QP and the tasks within the medical fields such as quality and risk management, clinical affairs, toxicology and biocompatibility. Anette is a member of the Swedish (TK355) and the international Technical (TC210) committees since 2010. Since 2003 Anette is […]
Lena Baard
Lena Baard, the founder and proprietor of Florian Consulting AB, boasts over a decade of experience working with sterile medical devices. With a rich work-life background spanning more than 20 years in the Life Science industry, she has gained extensive expertise in both pharmaceutical manufacturing and Medical Device Manufacturing companies. Lena possesses specialized knowledge in […]
Maria Axelsson
Maria has 25 years of quality experience in Life Science Industry, working with Pharmaceuticals, Medical devices, IVDs, and also the food industry. As an experienced trainer and qualified lead auditor, she combines deep regulatory knowledge with practical insights to deliver engaging workshops and courses. She provides trainings in several areas such as Auditing, Validation/Qualification, GMP […]
Sara Falkenklint
Sara Falkenklint is an experienced QA Manager and Trainer, with 20 years of experience within GMP and the pharmaceutical industry. She has expertise in quality and risk management, Quality Assurance, Quality Control labs, ATMPs, biologics, supplier management, audits/inspections, and process improvement. By combining theoretical knowledge with her hands-on experience, Sara delivers interactive courses that engage […]
Marika Lundin
Marika has a scientist background (PhD in Virology) and more than 10 years of experience in the Life Science industry, working in a variety of roles in different industry segments; eg Pharma / ATMP (eg Quality assurance, validation, qualification, production processes, aseptic assurance), contract research (project manager, product owner, sr scientist), IT (Business development and AM […]
Anna Sahlholm
Anna Sahlholm is employed at GBA Key2Compliance and has more than 15 years of experience from product and process development in close collaboration with research and within the medical device industry. Anna has worked with research, product development, strategic product management, clinical evaluations, processes for traceability, risk management, quality, and regulatory compliance for a variety […]
Susanne Grimsby
Susanne is one of our senior consultants, dedicated to supporting medical device and in vitro diagnostic (IVD) companies through a wide range of projects and training programs. She has a solid background from research and the life science business and with over 10 years of hands-on experience in QA/RA along, she brings a unique blend of technical expertise and practical insight to every project. Throughout her career, […]
James L. Vesper
Dr James L. Vesper designs and develops instructional courses and workshops for the pharmaceutical industry. He established and is president of the firm, LearningPlus, Inc., and has had more than 25 years’ experience in the pharmaceutical industry. Dr Vesper worked eleven years at Eli Lilly and Company, Indianapolis. His last assignment was as Project Leader […]