Timothy Wileman
About Timothy Wileman
Timothy Wileman is the Associate Director of Strategy and Business Operations Research & Development Quality at Bristol Myers Squibb, with over two decades of experience in pharmaceutical quality management and regulatory affairs.
Current Position at Bristol Myers Squibb
Timothy Wileman serves as an Associate Director for Strategy and Business Operations in Research & Development Quality at Bristol Myers Squibb. In this role, he contributes to the strategic direction and operational efficiency of the company's R&D quality initiatives. His responsibilities include overseeing compliance measures, ensuring the integrity of research operations, and fostering continual improvement in quality management processes.
Career at Celgene
Timothy Wileman had a distinguished career at Celgene, lasting from 2008 to 2022 in various capacities. He began as a Compliance Manager at the company's Stockley Park location, focusing on regulatory compliance. Later, he took on roles such as Lead Auditor for Pharmacovigilance (PV) and Associate Director for GVP Corporate Audit. Throughout his tenure, Timothy had a significant impact on Celgene's audit and compliance functions. His work helped ensure adherence to global regulations and bolstered the company’s quality management system.
Early Career in Quality Management
Timothy Wileman embarked on his career in quality management as a Temp Chemist at GKN Aerospace in 1995. He gained further industry experience as a Stability Analyst at Napp Pharmaceuticals from 1997 to 2000. He then moved on to Oxford GlycoSciences, where he worked as a Quality Officer from 2001 to 2004. During the early 2000s, his roles evolved, including positions as Snr Quality Associate at UCB and Quality Manager at Plethora Solutions and Pharmion, where he honed his expertise in regulatory affairs and quality assurance.
Educational Background in Applied Chemistry
Timothy Wileman completed his education at De Montfort University, where he earned a Bachelor of Science degree in Applied Chemistry. His academic pursuit lasted from 1990 to 1995. This solid foundation in chemistry provided him with the technical knowledge crucial for his later roles in quality management and compliance within the pharmaceutical industry.
Expertise in Pharmaceutical Quality Management
With over two decades of experience in the pharmaceutical industry, Timothy Wileman has a comprehensive background in quality management and regulatory affairs. He has held various pivotal roles, from Stability Analyst to Associate Director, showcasing his aptitude for maintaining and improving quality standards. His long-term commitment is evident from his extensive tenure at multiple organizations, where he contributed significantly to audit and compliance functions.