Teams at CSL

Lead CMC strategy and execution for pharmaceutical/biologic programs across development and early commercialization. Support process and analytical development, manufacturing tech transfer with CDMOs, GMP compliance, and author CMC regulatory submissions. Manage risks, partner relationships, and cross-functional stakeholders to meet quality, regulatory, and business objectives.

Lead global human factors strategy for medical devices and combination products. Embed HF in design controls, run formative and summative usability studies, perform risk assessments per ISO 14971, support regulatory submissions (FDA, EU MDR), collaborate cross-functionally, and mentor junior staff to ensure safe, effective, and user-friendly products.

Lead site Continuous Improvement (CI) for Bern site, advancing COS and implementing CI initiatives across GMP workflows. Drive KPI-based performance management, facilitate Lean/Six Sigma problem-solving, manage process optimization and digitalization (SAP/MES/TrackWise), coach stakeholders, and embed sustainable operational excellence aligned with global standards and regulatory requirements.