NewLimit is a biotechnology company working to radically extend human healthspan. We’re developing medicines to treat age-related diseases by reprogramming the epigenome, a new therapeutic mechanism to restore regenerative potential in aged and diseased cells. We leverage functional genomics, pooled perturbation screening, and machine learning models to unravel the biology of epigenetic aging and disease using experiments of unprecedented scale.
PositionNewLimit is seeking a scientist to drive our mRNA production and engineering efforts. This is a hands-on, lab based role focused on the synthesis, purification, and characterization of mRNA at large scales and high purities. You will serve as the technical lead for our production workflow, bridging the gap between molecular design and high quality material generation for in vivo and in vitro studies.
What you'll doAs a member of our team, you will:
- Execute and scale end-to-end mRNA production, including template preparation, in vitro transcription (IVT), and purification (TFF, chromatography).
- Implement rigorous quality control assays, including direct RNA sequencing, fragment analysis, dsRNA quantitation, and residual contaminant analysis.
- Author and maintain detailed SOPs and batch records, ensuring all production runs meet GLP standards.
- Independently design and execute experiments to improve mRNA sequence potency, specificity, and manufacturing performance.
- Train, manage, and mentor other team members on mRNA optimization and production workflows.
- PhD in molecular biology, biochemistry, cell biology, or a related field or equivalent industry experience (5+ years).
- Deep hands-on experience with IVT and the specific challenges of scaling nucleic acid production.
- Proficiency with TFF and chromatography systems for the purification of large scale RNA batches.
- Ability to perform and interpret mRNA QC assays and troubleshoot mRNA production challenges.
- Strong experience in drafting technical reports and standardized protocols.
- Familiarity with Python or R for sequence analysis and secondary structure prediction.
- Understanding of how mRNA quality attributes impact Lipid Nanoparticle (LNP) formulation and delivery.
- Experience with complex plasmid design and bacterial scale-up for DNA template generation.
- Experience managing external contract manufacturing organizations (CMOs)
NewLimit offers generous benefits to ensure our team can focus on our mission:
- Health, dental, and vision insurance
- 401(k) with company match
- Paid parental leave
- Industry-leading paid time off (PTO) — 20 days/year for all employees + holidays
- Meals and snacks on-site
Salary Range: $170,000 to $200,000. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. NewLimit offers a competitive benefits package, which includes a 401k, healthcare coverage, and 20 days of PTO. Learn more at: https://www.newlimit.com/careers *This compensation and benefits information is based on Company's good faith estimate as of the date of publication and may be modified in the future.
Skills Required
- PhD in molecular biology, biochemistry, cell biology, or related field or equivalent industry experience
- Deep hands-on experience with IVT and scaling nucleic acid production
- Proficiency with TFF and chromatography systems for RNA purification
- Ability to interpret mRNA QC assays and troubleshoot production challenges
- Strong experience in drafting technical reports and standardized protocols
What We Do
NewLimit is a biotechnology company working to radically extend human healthspan. We’re developing medicines to treat age-related diseases by reprogramming the epigenome, a new therapeutic mechanism to restore regenerative potential in aged and diseased cells. We leverage functional genomics, pooled perturbation screening, and machine learning models to unravel the biology of epigenetic aging and disease using experiments of unprecedented scale.
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