Take a leading analytical role across project and product portfolio
Ensure analytical methods remain compliant, robust, and fit for purpose
Drive method transfers, validations, and continuous improvements
Coordinate stability studies and support investigations and quality activities
Act as an Analytical Subject Matter Expert (SME)
Requirements
MSc/PhD, analytical chemistry/chemistry/biochemistry/pharmacist/chemical engineering or similar
+5 years of experience of Life Science/Pharma industry with commercial products
Experience of analysis of biological drugs, validation, analytical tech transfer, stability studies, specifications, handling of reference standards and critical reagents.
Skilled in common QC methods in the laboratory, e.g. any of HPLC, spectroscopy, ELISA, bioassay
Experience of working with contract manufacturer with CMOs and CLOs
Experience of GMP
English is required and Chinese highly preferred.
Benefits
Emphasis on work/life balance
Collaborative and team-oriented environment
Opportunities for professional growth
Diversity and Inclusion
Competitive compensation for your work
Making a positive impact to help ultra-rare disease patients who are in need of life saving treatments