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Manager Analytical Development

Job in Greater London, London, Greater London, W1B, England, UK
Listing for: BioTalent
Full Time position
Listed on 2026-09-14
Job specializations:
  • IT/Tech
  • Research/Development
Salary/Wage Range or Industry Benchmark: 90000 - 120000 GBP Yearly GBP 90000.00 120000.00 YEAR
Job Description & How to Apply Below
Location: Greater London

We are currently seeking an experienced Group Leader, Analytical Development to provide technical leadership across a portfolio of monoclonal antibody (mAb) programmes for a fast-growing biosimilars organisation in London.

This is a high-impact role focused on biosimilarity assessment, analytical strategy, and advanced molecule characterisation
, working closely with cross-functional teams to support development and regulatory activities. The position offers significant visibility and the opportunity to help shape scientific capability within a growing R&D environment.

Please note, this position is 5 days on-site (non-negotiable).
Visa sponsorship may be available for exceptional candidates based in the EU.

Key Responsibilities
  • Lead analytical development activities for biosimilar mAb programmes.
  • Drive biosimilarity and analytical similarity assessment strategies.
  • Provide technical oversight of HPLC methods including CEX, SEC, Glycan, HIC and Protein

    A.
  • Interpret LC-MS and advanced characterisation data.
  • Support capillary electrophoresis techniques including cIEF and CE-SDS.
  • Contribute to regulatory submissions and CMC documentation.
  • Act as a subject matter expert in cross-functional project reviews.
  • Mentor and develop analytical scientists.
  • Identify and implement innovative analytical technologies and approaches.
Requirements
  • Strong experience in analytical development of biologics or biosimilars
    , ideally monoclonal antibodies.
  • Expertise in analytical similarity assessment and molecule characterisation.
  • Hands-on knowledge of HPLC platforms, CE techniques and mass spectrometry data interpretation.
  • Experience supporting regulatory submissions and analytical CMC documentation.
  • Proven ability to provide technical leadership and mentor scientific teams.
  • Strong understanding of PTMs, impurity profiling and analytical method development.
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