Brian Turley
About Brian Turley
Brian Turley is a Validation Engineer with extensive experience in the pharmaceutical and biotechnology industries, currently working at Bristol-Myers Squibb and Valsource.
Current Position at Bristol-Myers Squibb
Brian Turley holds the position of Validation Engineer at Bristol-Myers Squibb. His responsibilities likely include validating systems, equipment, and processes to ensure compliance with regulatory standards and internal quality requirements.
Role at Valsource
Brian Turley is currently working at Valsource where he serves as both an Engineer and Validation Engineer. His extensive experience in the field likely contributes to his responsibilities in ensuring validation processes meet industry standards.
Experience at Alexion Pharmaceuticals
In 2015, Brian Turley worked as a Supervisor in Central Services at Alexion Pharmaceuticals, Inc. for a period of 11 months. His role would have involved overseeing central services operations and ensuring compliance with regulatory standards.
Previous Role at Genzyme
From 2013 to 2014, Brian Turley worked at Genzyme, a Sanofi company, as a Validation Lead for one year. His role involved leading the validation activities to ensure that systems and processes adhered to industry regulations and standards.
Extensive Tenure at Pfizer PGM
Brian Turley spent two decades at Pfizer PGM, holding a supervisory role from 1986 to 2006. During his 20-year tenure, he would have acquired significant expertise in supervisory practices and pharmaceutical operations.
Management Position at Amgen
Brian Turley served as a Manager at Amgen from 2005 to 2007 for two years. His management role would have entailed overseeing departments, ensuring compliance with regulatory standards, and contributing to operational improvements.
Professional Experience in Validation
Brian Turley has considerable experience in the pharmaceutical and biotechnology industries. He has worked at companies such as Genzyme, Lonza, and Alexion Pharmaceuticals, primarily focusing on validation roles, ensuring that systems and processes meet regulatory and quality standards.