Supervisor- Drug Manufacturing And Logistic Support.
Current• Delivered FDA, MHRA & OSHA compliance to the end drug user. Provided drug Manufacturing, GMP Equipment preparation and Warehouse Logistics expertise to various employer sites. • Supervised and prepared manufacturing and storage areas for FDA and MHRA audits.• Facilitated creation of production plans and shipping schedules in coordination with relevant GMP production teams.• Performed annual employee performance reviews from a GxP, Warehouse management and Ethics perspective.• Managed GMP production and Warehousing teams from 3 to17 employees through the employment tenure.• Performed Classroom training and On Job training for new hires relevant to warehouse and GMP processing.• Developed cGMP curricula related to Production and Warehouse operations. Documented training and retained as per GDP.• Processed incoming and outgoing inventories of drug APIs, manufacturing related components, Hazardous materials and Production equipment.• Managed ordering of all GMP gowning, production related components, prepared the requisitions and maintained the inventories facilitating Solid Dosage, Packaging, Aseptic, Clinical Trial, R&D and Softgel departments.• Coordinated between 5 sites to facilitate the equipment movement for storage, usage and cleaning.• Coordinated with Supervisors, Managers and Project leaders to schedule disinfection and sanitization of relevant areas. • Facilitated releases of all manufacturing materials and equipment based on scheduling requirements.• Supervised the production equipment disassembly, GMP equipment cleaning and reassembling. • Prevented API residue contamination via designing smart, detailed and exhaustive cleaning procedures and methods.