Liz Bastian's Email & Phone Number

💼 Past Experience

Liz Bastian most recently was a Regulatory Affairs Manager at Sunstar Americas, Inc in the Greater Chicago Area from September 2016 to May 2017 (9 months). Liz Bastian previously worked at Mapi Group from December 2015 to August 2016 (9 months) in Toronto, Canada Area. Liz Bastian also worked at Johnson & Johnson from August 2012 to November 2015 (3 years 4 months) in Toronto, Canada Area.

🎓 Education

Liz Bastian is currently a full-time graduate student at the University of Toronto, in Project Management and Biotechnology. She has been working with Pharma companies since she was in college, starting out as a Research Scientist. Liz Bastian holds a Master of Science from the University of Toronto in Project Management, Biotechnology and has also received a Bachelor of Science from Bharathiar University in 2003. Liz Bastian has been a Pharmaceutical Regulatory Affairs and Pharmaceutical Sciences Practitioner for over 10 years and has worked in laboratories for over 6 years. Liz Bastian has a strong background in Ophthalmology, and has experience in developing and testing new products and products in the market. Liz Bastian is currently working on her PhD at the University of Toronto, researching the efficacy of novel Eyesight Drugs.

💡 Technical & Interpersonal Skills

Liz Bastian is a Senior Regulatory Affairs Consultant at Mapi Group from September 2016 to May 2017 (9 months) in Toronto, Canada Area. Liz Bastian will provide regulatory compliance consulting to Sunstar Americas, Inc. in the Greater Chicago Area. Liz Bastian has experience with interacting with FDA for Class II and III medical devices and OTC and ANDA drug product submissions. Liz Bastian will also be responsible for providing expert regulatory strategy/guidance to staff and inter-disciplinary project teams. Liz Bastian will also be responsible for coordinating and attending pre-submission meetings with FDA. In addition, Liz Bastian will be a Primary point of contact for FDA on U.S. submissions. Liz Bastian is also responsible for facilitating product development of Class II and III medical devices and OTC and Rx drug product submissions. In addition, Liz Bastian will work with R&D Scientists and Engineers to plan, develop and execute new products, methods, technologies, and acceptance criteria. Additionally, Liz Bastian will evaluate experimental data, interpret results, write or critically review summary reports.