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Delivery Scientist

Job in Greater London, London, Greater London, W1B, England, UK
Listing for: FinalDose
Full Time position
Listed on 2026-10-11
Job specializations:
  • Pharmaceutical
    Pharmaceutical Science/ Research
Salary/Wage Range or Industry Benchmark: 65000 - 90000 GBP Yearly GBP 65000.00 90000.00 YEAR
Job Description & How to Apply Below

Final Dose's platform requires delivery solutions tailored to each therapeutic indication. You will lead delivery engineering across multiple administration routes, optimizing lipid nanoparticle formulations for tissue-specific targeting and therapeutic efficacy. Your work will bridge in vitro formulation development with in vivo validation and ultimately support technology transfer for GMP manufacturing. This is a critical role linking our construct engineering with clinical-stage drug products.

Responsibilities
  • Lead LNP delivery engineering across multiple administration routes, including local, systemic, and inhaled formulations
  • Develop and optimize LNP formulations with full physicochemical characterization (DLS, encapsulation efficiency, zeta potential)
  • Perform in vitro delivery optimization and hand off validated formulations to the in vivo team for animal studies
  • Support CMO/CDMO selection and technology transfer for GMP-grade manufacturing
  • Collaborate with biology teams to evaluate delivery efficiency using functional readouts (editing efficiency, reporter assays) in cell lines and primary cells
Required
  • Ph.D. in pharmaceutical sciences, drug delivery, biomedical engineering, or chemical engineering
  • 3–5+ years of hands‑on experience with lipid nanoparticle formulation
  • Demonstrated expertise in at least two of the following: mRNA‑LNP encapsulation and delivery, tissue-targeted delivery (SORT technology or ionizable lipid screening), inhaled or pulmonary drug delivery
  • Experience with microfluidic mixing and formulation scale‑up
  • In vitro delivery characterization in cell lines and primary cells
Preferred
  • Experience with intravesical or local drug delivery
  • CMC or technology transfer experience with a CDMO
  • Air‑liquid interface (ALI) culture and aerosol delivery expertise
  • Awareness of GMP manufacturing processes and requirements
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