Simon B.

Simon B.

Associate Director Regulatory Affairs @ Bristol Myers Squibb

About Simon B.

Simon B. is the Associate Director of Regulatory Affairs at Bristol Myers Squibb in Melbourne, Australia, with over 25 years of experience in the pharmaceutical industry.

Title

Simon B. currently holds the position of Associate Director Regulatory Affairs at Bristol Myers Squibb. He began this role on January 1, 2020.

Current Company

Simon B. is presently employed at Bristol Myers Squibb, a global biopharmaceutical company headquartered in the Melbourne CBD, Victoria, Australia. In his role as Associate Director Regulatory Affairs, he focuses on ensuring regulatory compliance and managing regulatory submissions.

Work Experience at Celgene

Prior to his current role, Simon B. worked at Celgene as Director of Regulatory Affairs from 2017 to 2020 in Melbourne, Australia. During his three-year tenure, he was responsible for overseeing regulatory strategies and submissions to support the development and approval of Celgene's pharmaceutical products.

Tenure at Amgen Australia Pty Ltd

Simon B. spent a significant portion of his career at Amgen Australia Pty Ltd, spanning over 12 years in various roles. From 2005 to 2009, he served as Compliance Manager and Senior Manager, focusing on compliance and regulatory standards. From 2009 to 2017, he held the position of Regulatory Affairs Senior Manager, where he played a key role in regulatory oversight and product approval processes.

Career at CSL

Simon B. worked at CSL in multiple roles over the course of seven years, including QA Manager (2004-2005), Senior Regulatory Affairs Associate (2003-2004), Regulatory Affairs Associate (1998-2003), and R&D Associate (1993-1998). His diverse responsibilities at CSL included quality assurance, regulatory affairs, and research and development.

Education and Background

Simon B. graduated from the University of Melbourne with a Bachelor of Science in Biochemistry, completing his studies from 1998 to 2001. He also attended Marcellin College from 1995 to 1997. He has accumulated over 25 years of experience in the pharmaceutical industry, working in regulatory affairs, compliance, drug safety, clinical quality assurance, and R&D.

Expertise in Regulatory Affairs and Compliance

Simon B. has extensive expertise in regulatory affairs and compliance. His experience includes senior positions at leading pharmaceutical companies such as Celgene and Amgen Australia Pty Ltd. His work has been integral to ensuring that products meet regulatory standards and gain necessary approvals.

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