Senior Scientist: RNA-LNP Formulation & Process Development

BioSpace

Boston (MA)

On-site

USD 72,000 - 216,000

Full time

31 hours ago
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Job summary

Lilly is seeking a skilled RNA-LNP scientist to design and execute experiments, develop scalable LNP processes, and ensure product quality across development stages. You will collaborate with cross-functional teams, interpret analytical data, and contribute to regulator-ready documentation.

Responsibilities include technology transfer support for early-stage CT manufacture, mentorship of juniors, and maintaining rigorous records while pursuing innovation in parenteral drug products.

Qualifications

  • Bachelor's degree with 4+ years in industry or equivalent.
  • Hands-on RNA-LNP formulation and downstream processing experience.
  • Authorized to work in the United States.

Responsibilities

  • Plan, design, and execute experiments; manage multiple priorities across CMC functions.
  • Develop and scale LNP manufacturing processes (rapid-mixing, tangential flow filtration).
  • Characterize process parameters vs. quality attributes (size, encapsulation, RNA integrity).
  • Present data at team meetings and conferences; communicate results clearly.
  • Support technology transfer for early-phase CT manufacture and site transfers.
  • Train and mentor junior scientists and maintain robust lab records.

Skills

RNA-LNP formulation
Data analysis
Communication
Problem solving

Education

Bachelor's degree in chemical engineering or related field
Master's degree in chemical engineering or related field

Tools

LNP processing
TFF
RiboGreen
UPLC/HPLC

Job description

Lilly is seeking a skilled RNA-LNP scientist to design and execute experiments, develop scalable LNP processes, and ensure product quality across development stages. You will collaborate with cross-functional teams, interpret analytical data, and contribute to regulator-ready documentation.

Responsibilities include technology transfer support for early-stage CT manufacture, mentorship of juniors, and maintaining rigorous records while pursuing innovation in parenteral drug products.

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