About the role
We are currently looking for an experienced analytical science professional specializing in analytical method validation and transfer to contract manufacturing organizations (CMOs/CDMOs). Strong focus on troubleshooting, root-cause investigation, and ensuring robust analytical performance across external laboratories and CMOs under GMP conditions. In this position you will be directly reporting to the CMC Strategy and Technology Transfer Lead.
Key Responsibilities
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
Core Expertise
Analytical method transfer strategies (internal labs and CMOs)
Analytical method development, validation, and lifecycle management
Advanced analytical techniques:
HPLC / UPLC
GC
Dissolution
Spectroscopy
Troubleshooting & deviation management (OOS/OOT investigations)
Data evaluation
GMP, ICH guidelines, and regulatory compliance
Professional Skills
Experience working with contract manufacturers (CMOs/CDMOs) in a global environment
Strong scientific problem-solving and troubleshooting mindset
Excellent communication skills for interfacing with internal teams and external partners
Structured and results-driven project management capabilities
High level of accountability, persistence, and attention to detail
Ability to manage multiple priorities in a regulated environment
Qualifications
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
About CSL Vifor
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.
To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.
Our Benefits
For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.
You Belong at CSL
At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.
To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging
Equal Opportunity Employer
CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.