This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Form part of a group of technical experts (SMEs) responsible for the continuity, quality, compliance, and profitability of the on-market Clinical Nutrition (pharmaceutical) portfolio. Lead and support the execution of product changes in compliance with international regulations and quality standards, working with cross-functional teams to ensure effective problem-solving, decision-making, and timely change implementation. The position combines strong technical expertise, project leadership, and people management responsibilities, driving lifecycle management activities and operational excellence across regions.
Job Responsibility
Manage routine and complex changes for the on-market Clinical Nutrition (pharmaceutical) portfolio
Mentor/lead a team of scientists responsible for lifecycle design and change execution activities for on-market products
Provide direction on prioritization, technical problem solving, and process clarification, ensuring alignment with organizational objectives
Plan, organize and execute product changes in compliance with global regulatory and quality requirements
Lead cross-functional teams and facilitate decision-making to ensure timely project delivery
Apply advanced scientific and cross-functional knowledge to drive outcomes
Utilize project management tools to manage timelines, risks, and budgets, while identifying and resolving issues impacting delivery
Establish and maintain metrics to track operational performance and KPIs
Communicate progress and results to management and Senior Leadership Team (SLT) as required
Drive market enhancements and operational improvements
Contribute to development and continuous improvement activities related to product design, manufacturing, and control
Requirements
Bachelor's degree (EQF Level 6) in a scientific discipline (Chemistry, Biology, Pharmaceutics, Chemical Engineering, or related) with 8+ year experience, or Master's degree (EQF Level 7) with 4+ year experience, or PhD (EQF Level 8) with 1+ year experience
Relevant experience in the pharmaceutical or other regulated industry, with a broad background in product development and lifecycle management
Fluent in English
Nice to have
Familiarity with analytical techniques and/or process engineering is advantageous