Global Program Head for Respiratory Programs in Sandoz Product Development.

Managing strategic projects with global impact in Technical Development / Pharmaceutical Development.

Head of global department for Oral Pharmaceutical Development. Management of 150 + associates in 3 global sites (US, Switzerland, India), organized in early and late phase development teams, lab-scale facility, and pilot plant for solid dosage forms. Budget responsibility for internal and external budget, capex planning and execution.. concurrent projects in all development phases (preclinical, early phase, confirmatory development, transfer and launch). Co-lead of development-manufacturing… Show more Head of global department for Oral Pharmaceutical Development. Management of 150 + associates in 3 global sites (US, Switzerland, India), organized in early and late phase development teams, lab-scale facility, and pilot plant for solid dosage forms. Budget responsibility for internal and external budget, capex planning and execution.. concurrent projects in all development phases (preclinical, early phase, confirmatory development, transfer and launch). Co-lead of development-manufacturing committee for project governance across line-functions. Show less

Head of development department for Inhaled Drug Products in Basel. Managed approx. 100 staff in analytical, pharmaceutical, and device development groups and a team of senior CMC project managers. Portfolio of ten + inhaled development projects in all development stages.

Technical Project Leader for Inhaled Drug Products. Represented Technical Research and Development in Global Program Teams. Owner of Technical Development Plan for assigned projects. Regular contributor to Integrated Program Strategy and Product Design Processes. Responsible for all aspects of CMC development: Pharmaceutical, Analytical, and Device Development, Regulatory Strategy, Clinical Trial Supply Planning, Manufacturing, and Logistics. Extensive experience with regulatory documentation… Show more Technical Project Leader for Inhaled Drug Products. Represented Technical Research and Development in Global Program Teams. Owner of Technical Development Plan for assigned projects. Regular contributor to Integrated Program Strategy and Product Design Processes. Responsible for all aspects of CMC development: Pharmaceutical, Analytical, and Device Development, Regulatory Strategy, Clinical Trial Supply Planning, Manufacturing, and Logistics. Extensive experience with regulatory documentation (Briefing books, IND/IMPD, Submissions). Show less

Project Leader for Pharmaceutical and Analytical Development of Inhalation products. Responsible for analytical and pharmaceutical process development. Ownership technical development plans and project budget planning and execution. Co-lead of Campus project to move Technical Development to new laboratories and offices on Campus in Basel for several TRD line-functions (~350 associates).

Head of Laboratory in Analytical Development group for Inhaled Drug Products. Development and validation of analytical methods, planning and execution of pharmaceutical development and stability studies at external partners and in-house.

Group Leader in Analytical Development for cGMP compliant analytical development and quality control of drug substances, drug products, and excipients. CMC representative in Global Program Teams. Leader of LC/MS laboratory for drug substance, drug product, and packaging characterization.

Laboratory Head in Analytical Development for cGMP compliant analytical development and quality control of drug substances, drug products, and excipients. Leadership roles in CMC development teams in the fields of specialized therapeutics and oncology. System owner for site-wide client server chromatography data system EMPOWER for approximately 300 users. Member in group of experts of German Pharmacopoeia (DAB) commission.