Jesse Duthrie, Pmp Email & Phone Number

Boulder, CO, US

Basel, BS, CH

• Manage commercial pharmaceutical projects by leading cross-functional teams in the delivery of manufactured APIs. Plan schedules, facilitate meetings, and identify risks to determine strategy with key stakeholders from.
• Lead pharmaceutical projects in clinical development. Oversee deliverables of milestones including technology transfers, method implementation and validation, stability studies and GMP manufacturing. Lead.
• Organize and maintain project costing tools. Budget resources (i.e. material, labor, equipment), update actual hours, and prepare forecasts for project lifecycle.
• Write work orders and change orders, manage invoicing of existing work with finance and supply chain teams.
• Perform impact assessments and scenario planning, provide recommendations to leadership team on course of action for resource and production planning.

Basel, CH

• Manage a team of five to create master batch records (MBRs) for biologic drug substance manufacturing at 200L, 1000L, and 2000L production scales.
• Successfully converted 200L pilot laboratory into a GMP facility. Led a cross-function team of 25 people to prepare GMP readiness for documentation, QC sampling, material management, training, and quality management.
• Led a cross-functional project of 20 members to extend shelf lives of raw materials using updated company guidelines. Total cost saved by extending shelf lives of materials was 5.5 million dollars (USD).
• Participate in internal and joint project team meetings, consult with program managers and customers from China, Europe, and America to align on Statements of Work, issue good receipts of services in SAP.
• Review team budget and plan headcount based on annual projection of technology transfers and repeat manufacturing batches.

Basel, CH

• Supported startup operations of a new manufacturing facility in Guangzhou, China. One of first 30 hires, worked with site head and department directors to prepare site of 400+ employees for GMP manufacturing.
• Authored MBRs for biologic drug substance manufacturing for early clinical and commercial customers. Knowledgeable in all process steps of biologics manufacturing (i.e. inoculation, fermentation, primary recovery.
• Member of project teams, worked regularly with customers and program managers to complete tasks.
• Coordinated technical discussions between subject matter experts (i.e. engineers, biotechnicians, scientists).

Basel, CH

Basel, CH

Chicago, US

Published marketing material including articles, interviews, and brochures.

US

Master Of Business Administration - Mba

Master Of Fine Arts (M.F.A.), Nonfiction Writing

Bachelor Of Arts (B.A.), English Language And Literature/Letters