Pharmaceutical Development & Manufacturing Technology Senior Scientist

--- base: meta-keywords: meta-viewport: width=device-width, title: Pharmaceutical Development & Manufacturing Technology Senior Scientist --- Pharmaceutical Development & Manufacturing Technology Senior Scientist ======================================================================= Within our Pharmaceutical Development Management department, you will lead pharmaceutical development projects, technology transfers, and product support for solid, semi-solid, and liquid forms. You will actively contribute to the optimization of manufacturing processes, technological innovation, and continuous improvement, while ensuring compliance with GMP and international regulatory requirements. Your responsibilities: * Manage pharmaceutical development and product support projects within defined deadlines, budgets, and objectives * Define product quality profiles and develop the specifications necessary for development * Plan, coordinate, and analyze galenic development studies and product support activities * Participate (if necessary) and supervise trials conducted in the galenic laboratory and in production * Coordinate activities with the Production, Quality Control, Quality Assurance, Regulatory Affairs and other involved departments and functions * Participate in the implementation and promulgation of the Quality by Design approach, risk analyses, as well as validation activities * Contribute to the preparation of technical documentation intended for health authorities * Identify and propose improvements in processes, equipment, and technologies * Ensure scientific and technological monitoring in order to develop internal expertise * Support Manufacturing during quality investigations if necessary * Train and support team members in their technical development * Provide necessary support during internal audits and regulatory inspections * University degree in pharmacy, pharmaceutical sciences, chemistry or an equivalent field * Significant experience in pharmaceutical development within a GMP environment, particularly in liquid/semi-solid forms (solid forms is a plus) * Solid knowledge of pharmaceutical formulation and manufacturing technologies * Excellent mastery of GMP, ICH requirements, and applicable international regulations * Experience in multidisciplinary project management * Critical and analytical thinking, solution-oriented, and ability to take initiative * Good statistical knowledge * Excellent communication and collaboration skills * Proficiency in English; French is an asset Opportunities for professional development and continuing education Corden Pharma International Switzerland GmbH * Corden Pharma International Switzerland GmbH Aeschenvorstadt 71 4051 Basel * [ ](< >) jpide568f5fjm jpit1041jm jpiy26jm