Graeme Lowe
About Graeme Lowe
Graeme Lowe is the Head of Global Pharma Operations, Internal Manufacturing Quality at Bristol-Myers Squibb, with extensive experience in quality management across multiple continents and a strong focus on Diversity & Inclusion.
Title
Graeme Lowe is currently the Head Of Global Pharma Operations, Internal Manufacturing Quality at Bristol-Myers Squibb. He operates in the Neuchâtel Area, Switzerland.
Company
Graeme Lowe is currently working at Bristol-Myers Squibb. His role involves overseeing internal manufacturing quality for the global pharmaceutical operations.
Previous Experience at Celgene
Graeme Lowe has held multiple significant roles at Celgene in Neuchâtel Area, Switzerland. He served as Vice President Quality, Internal Manufacturing in 2019-2020. Prior to that, he was Executive Director, Head of Internal Manufacturing Quality from 2018 to 2020, and also held the position of Executive Director, Global Head of Commercial Laboratory Operations from 2017 to 2018 in Boudry, Switzerland.
Career at Shire and Baxalta
At Shire, Graeme Lowe served as Quality Director, FQMR from 2016 to 2017 in Neuchâtel. Before that, he worked at Baxalta as Senior Manager Laboratories from 2015 to 2016, also in Neuchâtel.
Role at Catalent Pharma Solutions
Graeme Lowe was with Catalent Pharma Solutions in Swindon, United Kingdom, where he filled the positions of Director of Development and Analytical Solutions from 2011 to 2015, and Quality Control Manager from 2009 to 2011.
Early Career at Pfizer Ltd
Graeme Lowe started his substantial career at Pfizer Ltd as a Quality Control Manager, a role he held from 1993 to 2009.
Educational Background
Graeme Lowe studied Applied Chemistry, focusing on Organic Chemistry, Biochemistry, and Biotechnology, at The University of Huddersfield from 1988 to 1992.
Global Operational Experience
Graeme Lowe has extensive experience managing teams across multiple continents, including Asia, Europe, and North America. This involves overseeing quality operations at sites in Switzerland, the USA, China, and Japan, along with leading Qualified Person (QP) teams in the UK and Netherlands.
Regulatory Audits and Compliance
Graeme Lowe has significant experience with regulatory audits from agencies such as FDA, MHRA, ANVISA, and Swiss Medic. His roles have demanded stringent adherence to regulatory standards and compliance.
Focus on Diversity and Inclusion
Graeme Lowe has a strong focus on Diversity & Inclusion, especially in global roles where English is not the first language. This focus is integral to his leadership approach in diverse, multicultural teams.