↳Bachelor-s degree or equivalent in a scientific or quality-related field. Advanced degree preferred
↳Significant experience in the pharmaceutical / biotech / medical device industry, including knowledge of the end to end development and operationalisation of products, and the associated GxP regulations and considerations (e.g., GCP,GVP, IVD/MD Regulations)
↳Solid experience in leading GxP audits and managing complex quality projects
↳In-depth knowledge of drug development processes and global regulatory landscapes
↳Good understanding of Information Systems, e.g., audit management and analysis reporting tools
↳Fluency in written and spoken English; bi or multi-lingual skills are desirable
↳Clinical Operations experience or quality function in system validations
↳Leadership and Stakeholder Management: Demonstrates exceptional ability to influence, negotiate, and mentor while effectively managing relationships with diverse stakeholders in global settings
↳Analytical and Strategic Thinking: strong data and digital literacy, with the critical thinking ability to synthesize complex or ambiguous information into clear, actionable insights
↳Execution and Independence: Combines strong organizational and project management skills with the capacity to work effectively-both independently and collaboratively-within international, agile matrix organization
