Scientist, Analytical Science & Method Transfer

Lead and coordinate analytical method transfer activities to or between Quality Control laboratories and external contract manufacturers Act as SME (Subject Matter Expert) for analytical issues during technology transfer and commercial manufacturing of drug substances and drug products Perform scientific troubleshooting for analytical methods (e.g., HPLC, GC, spectroscopy) in response to OOS, OOT, and atypical results Support CMOs/CDMOs in establishing analytical methods, resolving analytical challenges, ensuring alignment with internal standards and regulatory dossiers In case of method transfer by revalidation: design, optimize, and validate analytical methods according to ICH guidelines and GMP requirements Review and approve method transfer protocols, validation reports, and analytical documentation Drive root cause analysis and define CAPAs for analytical deviations in collaboration with cross-functional teams Ensure consistent method lifecycle management, including continuous improvement and robustness enhancement Support regulatory submissions by preparing and reviewing analytical sections (e.g., CTD Module 3) for new laboratories and CMOs Act as a key interface for Analytical Science & Method Transfer between Technology transfer team, Quality Assurance, Regulatory Affairs, and external partners

CSL Vifor is a global partner of choice for pharmaceuticals and innovative, leading therapies in iron deficiency and nephrology. We specialize in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision healthcare, aiming to help patients around the world lead better, healthier lives. Headquartered in St. Gallen, Switzerland, CSL Vifor also includes the joint company Vifor Fresenius Medical Care Renal Pharma (with Fresenius Medical Care). The parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people and delivers its lifesaving therapies to people in more than 100 countries.

• Degree in Chemistry, Pharmaceutical Sciences, or related field (e.g., HTL, ETH, MSc or equivalent)

• Minimum 5 years of experience in analytical development or quality control within the pharmaceutical industry

• Proven track record in method transfer and analytical troubleshooting

• Solid knowledge of GMP, ICH, and ISO standards