• Lead and manage the advancement, evaluation, and manufacturing of solid dosage forms or combination products, encompassing clinical and market variations
  • Ensure sufficient and timely supplies for development projects based on input from the Global Supply Chain, CMC, Project, and/or Life Cycle management functions
  • Guide the technical phases of drug product development: strategize, coordinate, and manage the multifaceted technical operations essential for the evolution, expansion, validation, and production of a drug from its initial stages to commercial distribution
  • Lead the collaboration with external development partners with special emphasis on cost efficiency, timelines, and scientific quality
  • Ensure compliance with regulatory guidelines


  • Pharmacist or equivalent holding a PhD, with a minimum of 10 years of relevant working experience in the pharmaceutical industry
  • Minimum of 5 years of experience leading an interdisciplinary drug product team
  • Scientific expertise in parenteral formulations and formulations for combination products OR expertise in small molecule formulation development and in oral solid dosage forms
  • Profound knowledge in QbD, DOE and QRM
  • Excellent proficiency in English, both verbal and written