Alexandra Steib is a Senior Drug Regulatory Affairs Consultant with over 20 years experience working in the Pharmaceutical and Biotechnology Industry within small, medium and large organizations, both as an employee and consultant. Throughout her career she developed an in-depth knowledge on all aspects of drug development, quality systems and regulatory project management across Canada, the United States and Europe with strong quality and compliance focus, high attention to detail, and a proven track record of timely delivery.
Highly experienced in drug regulatory submissions and affairs, she has vast experience with the regulators, globally acting pharmaceutical companies, and drug products. She is well versed in drug development, clinical development, biotechnology and immunology. Alexandra successfully built high performance RA teams and fostered key relationships with companies, their customers, partners, vendors, as well as with regulatory agencies and industry group. Alexandra has worked for pharmaceutical companies in Germany, Switzerland, UK, Canada, and the US.
Alexandra has a solid scientific background holding a PhD in Veterinary Medicine from Ludwig-Maximilians University in Munich, Germany, and she is also a member of the Royal Society of Biology in the UK. When not working she enjoys travel and reading. She is fluent in English and German, and lives in Toronto, Ontario, Canada.
The International Society of Female Professionals Member Alexandra Steib, PhD, can be found on the Who’s Who Directory, where she is looking forward to networking with you.