Senior Scientist (new Modalities) – Analytical Science & Technology, Global Product Development, Pt&d

AstraZeneca

Macclesfield, , GB
Soft-matter material science expertise
Physical chemistry and biophysics application
Material characterisation techniques
AstraZeneca is a global, science-led, patient-centred biopharmaceutical company focusing on discovering, developing, and commercialising prescription medicines for serious diseases

Job Summary

  • AstraZeneca is a global, science-led, patient-centred biopharmaceutical company focusing on discovering, developing, and commercialising prescription medicines for serious diseases.
  • The Senior Scientist will strengthen capabilities in material science applied to next generation therapeutics, working across peptides, oligonucleotides, siRNA-conjugates, biologics, and other complex modalities.
  • The role involves combining theory, lab experimentation, and modelling to understand material attributes influencing drug product performance and manufacturing robustness.

Matching Summary

AstraZeneca is a global, science-led, patient-centred biopharmaceutical company focusing on discovering, developing, and commercialising prescription medicines for serious diseases.

Skills & Requirements

Must-have

  • Soft-matter material science expertise
  • Physical chemistry and biophysics application
  • Material characterisation techniques
  • Drug product process understanding
  • Digital-first modelling and simulation
  • Collaboration with cross-functional teams

Nice-to-have

  • Experience with lyophilised drug products
  • Molecular dynamics modelling
  • Familiarity with NMR and Raman techniques
  • Outsourced partner management
  • Regulatory document authoring
  • AI tool development for material characterisation
  • Working under GLP/GMP standards

Key Requirements

  • PhD or MSc/BSc with industrial experience
  • Experience with large molecule material behaviours
  • Knowledge of SEC-MALS, DLS, AF4, DSC, and rheology
  • Proven leadership in multidisciplinary scientific teams
  • Strong communication skills
  • Experience under GLP/GMP standards
  • Experience with CMC regulatory authoring

Work Rights

Not specified

Tailored Resume

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