Susan Gillham
About Susan Gillham
Susan Gillham is a Manager of GxP IT Audit (IT Quality Assurance) at Bristol-Myers Squibb, with extensive experience in quality control, regulatory compliance, and IT systems auditing.
Title
Susan Gillham currently holds the position of Manager, GxP IT Audit (IT Quality Assurance) at Bristol-Myers Squibb. In this role, she works as a remote auditor based in Henderson, KY. Her responsibilities include planning, organizing, executing, and documenting audits of regulated computerized systems and related IT controls.
Current Role at Bristol-Myers Squibb
Susan Gillham is currently employed at Bristol-Myers Squibb as Manager, GxP IT Audit (IT Quality Assurance). She focuses on providing advice, training, and counsel concerning computer system regulatory requirements to staff and business stakeholders on computerized system/validation projects. Her role also involves reviewing and assessing corrective and preventive action plans to ensure compliance with relevant e-record and e-signature regulations.
Previous Experience at Bristol-Myers Squibb
Susan Gillham has held various roles at Bristol-Myers Squibb throughout her career. She worked as GLP Auditor/Senior Auditor, R&D Global Quality & Regulatory Compliance from 2014 to 2016 in Mt. Vernon, IN. Prior to that, she was a Research Scientist II for 13 years from 2001 to 2014. Additionally, she served as a Quality Control Laboratory Analyst for 5 months in 2000-2001 in Mt. Vernon, IN.
Early Career and Education
Susan Gillham started her career as a Phlebotomist I at Methodist Hospital of Henderson, Kentucky, where she worked for one year from 1999 to 2000. She studied Animal Health and Veterinary Sciences/Agriculture at Murray State University, achieving a degree in Animal Health Technology (Area) from 1993 to 1997.
Expertise in IT Quality Assurance and Compliance
Susan Gillham has extensive experience in conducting internal, external vendor, and on-site FDA inspections. She possesses vast knowledge in computerized systems compliance, histology, and immunohistochemistry procedures and practices. Her expertise extends to advising on regulatory requirements for computer systems and ensuring adherence to e-record and e-signature regulations.