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Life Science Talent Logo Life Science Talent · Research and Development

Senior Research Scientist - Peptide Chemistry & Formulation

Sweden, Lund Employment contract · Job Posted June 29, 2026
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Job Description

We are seeking a Senior Research Scientist to join our Pharmaceutical Research & Early Development team in Lund. This is a technically demanding role at the intersection of peptide chemistry, lipid-based formulation science, and analytical characterization. You will work with Camurus’ proprietary FluidCrystal® delivery technology and other formulation technologies to develop and advance novel formulations for peptide-based drugs through the early-to-clinical development pipeline. This is a unique opportunity to contribute to the development of next-generation therapies that have a direct impact on clinical-stage programs.

Job Responsibility

  • Design, develop, and optimize formulations for peptide APIs using Camurus’ FluidCrystal® platform and other formulation technologies as appropriate
  • Develop and refine formulation strategies including long-acting injectable and depot systems
  • Evaluate internal and external assets and formulation approaches to support business development activities
  • Contribute to CMC sections of IND/CTA and NDA/MAA regulatory dossiers
  • Support technology transfer activities to internal manufacturing operations and external partners
  • Act as a scientific expert in cross-functional project teams spanning R&D, quality, and manufacturing
  • Keep up to date with developments in peptide drug delivery, formulation science, and relevant analytical technologies

Requirements

  • M.Sc. or Ph.D. in organic chemistry, pharmaceutical/medicinal chemistry or a closely related discipline
  • Minimum 5 years of post-doctoral or industrial experience in peptide chemistry, with demonstrable expertise in both formulation development and analytical characterization
  • Strong understanding of peptide degradation mechanisms (hydrolysis, oxidation, racemisation, aggregation) and experience with stability assessment and optimization
  • Track record of contributing to CMC regulatory dossiers (IND/CTA or NDA/MAA), with familiarity of ICH Q8–Q11 guidelines
  • Experience working in structured, cross-functional project teams with demonstrated ability to deliver results independently

Nice to have

  • Experience with lipid-based drug delivery systems, or other advanced parenteral/depot long-acting drug delivery platforms
  • Experience in a GMP-regulated environment and knowledge of ICH Q6B specifications for peptide/biotech products
  • Understanding of biopharmaceutics and PK/PD relationships relevant to peptide drugs and controlled-release systems
  • Experience with technology transfer to manufacturing or external partners (CMOs/CROs)

What we offer

  • International work environment and corporate culture
  • Possibility for individual development and growth
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