Charles Willoughby
Supervisor, Manufacturing Support at Kbi Biopharma @KBI Biopharma
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WORK HISTORY
Supervisor, Manufacturing Support at Kbi Biopharma @KBI Biopharma
Durham, NC, US
As a Supervisor in the Manufacturing Support Department I coordinate and supervise, Manufacturing Support operations such as Cleaning of the GMP Facilities, PAR operations, Raw Material Sampling operations and Process Waste Operations. I ensure compliance in all operations that align with all regulatory guidelines, company policies, Standard Operating Procedures (SOP) and Policy Documents (PD). I also supervise and support all Manufacturing Support operations accurately and apply their GMP knowledge and experience to troubleshoot operational issues. This includes facilitating additional support with external departments, such as responses required to maintain and ensure all Manufacturing Departments are operational which may require work schedule adjustments. It is my job to guide, mentor and coach Manufacturing Support personnel ensuring each associate understands their daily task, performs their task with extreme efficiency, and coach them to exceed all expectations and gives each associate the tools to become successful. As a Supervisor of the Support Department I maintain a sense of ownership of all the Support Department operations for my shift and ensure the resources are available, resources are coordinated, resources are efficient, and Quality is implemented in all aspects of the Support Department. I am efficient in the use of the Quality System (CAPA, Deviation, Change Control, and Training) this ensures compliance within the Department. It is the expectation as the Supervisor of the Manufacturing Support Department to lead by example and to model the KBI Values. It is my duty as a Supervisor to ensure the safety and compliance of each personnel while on KBI property.
ABOUT CHARLES WILLOUGHBY
Over 16 years of experience in pharmaceutical manufacturing with the same employer and over 27 years of experience in the pharmaceutical industry. Thorough understanding of Lean Manufacturing processes Strict adherence to housekeeping, safety, and cGMP and ISO procedures Excellent leadership and training skills Attentive to details for regulatory compliance and documentation Strong communication and interpersonal skills Successful completion of various training courses and exams Efficient in Microsoft Word and Outlook, ABB/DCS/PCS process control system, Delta V, Unicorn, and Lotus • NC State certified for Bioprocessing Technology • Work Keys Certified • Knowledge of cGMP guidelines
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