Drive reliable clinical trial supply planning and ensure drug product availability across global studies
Create and maintain production plans in alignment with the production facilities in relevant planning systems
Secure drug product availability to enable execution of clinical trials according to supply strategies
Balance supply and demand within inventory policies to minimise waste
Optimise trial usage of batches based on remaining shelf life, quantity, and FEFO principles
Coordinate forecasts, order confirmations, and batch release with relevant production and supply stakeholders
Chair supply and demand meetings with key internal stakeholders
Maintain accurate planning data in relevant systems
Identify and contribute to process improvements within the team and department
Ensure compliance with internal procedures, standards, and relevant GMP/GCP requirements
Requirements
Bachelor’s or master’s degree within Supply Chain Management, Engineering, Logistics, Economics, Operations Research, Mathematics, Statistics, or a related field
Hands-on experience with supply chain planning, logistics planning, inventory planning, demand/supply planning, batch planning, production planning, or similar
Experience working with planning processes where timing, lead times, stock levels, and availability are important
Strong analytical skills and are comfortable working with data, assumptions, scenarios, and planning tools
Can coordinate with stakeholders across functions and follow up to ensure progress and alignment
Solid system skills and are confident working with Microsoft Office and planning-related systems
Communicate clearly in English, both written and spoken
Fluent in Danish or able to work effectively in a Danish-speaking team environment