ANALYTICAL DEVELOPMENT GROUP LEADER
Biosimilar mAb Characterisation Strategy
London | On-site | Monday - Friday
Visa Support Available: International Applicants Encouraged to Apply
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BioTalent are partnered with a growing biopharma organisation strengthening its analytical development capability within a global biosimilars portfolio. This is not routine analytical testing. This is about building and defending a robust biosimilarity and analytical similarity strategy across monoclonal antibody programmes. The focus is deep molecule-level understanding, structural characterisation and regulatory-defensible data packages.
The Role
You will lead analytical development strategy for biosimilar mAbs, with responsibility across:
β’ Analytical similarity and biosimilarity assessment frameworks
β’ Comprehensive physiochemical characterisation of monoclonal antibodies
β’ Establishment and optimisation of HPLC methods including: Glycan profiling, CEX, SEC, Protein A, HIC
β’ Capillary electrophoresis techniques including cIEF and CESDS
β’ LCMS data interpretation for PTM identification and structural analysis
β’ Impurity profiling and degradation pathway assessment
β’ Method development, qualification and lifecycle management
β’ Statistical analysis and use of DoE in analytical method optimisation
β’ Support of Module 3 analytical content for IND, IMPD, BLA and MAA
β’ Interaction with Regulatory Affairs on EMA, MHRA and FDA queries
You will act as the analytical SME in cross-functional stage gate reviews, challenging interpretations and ensuring analytical conclusions are scientifically defensible. This role is technical leadership rather than daily wet-lab execution. You may not run assays yourself every day, but you will design the strategy, review the data and direct the technical path.
Essential Experience
β’ Direct biosimilars analytical development experience
β’ Demonstrated experience in analytical similarity and biosimilarity assessment
β’ Strong understanding of mAb structure, PTMs and higher-order structure
β’ Deep expertise across HPLC and CE platforms
β’ Ability to interpret LCMS data for structural differences
β’ Experience supporting regulatory submissions with analytical content
β’ Experience leading or mentoring analytical scientists
This is not suitable for:
β’ QC analysts focused on release testing
β’ Small molecule analytical chemists
β’ Scientists without biosimilars exposure
β’ Pure people managers lacking technical depth
Why Move
In biosimilars, analytical similarity is the battleground. This role owns how molecules are characterised, compared and defended. It is a high-visibility position within a growing technical site backed by global experience.