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Research Scientist, Lipid Chemistry

GenScript/ProBio

Redmond, WAOnsitePosted 35 days ago$90,000 - $110,000/year
Full TimeEntry LevelResearch & ScientistCDMO
Original posting ↗

Summary

GenScript has a customized RNA synthesis and delivery formulation service established with good growth opportunity. We are looking for a highly motivated and scientifically rigorous individual to join our Innovation Center for novel lipid or other polymer molecules development to be used in RNA and gene delivery formulation, with experience in developing organic lipid and polymer molecules from R&D to Scale up.

Job description

Duties/Responsibilities

  • Everyday hand-on chemist willing to get into laboratory to conduct novel organic and lipid polymer chemical synthesis to support and build the company’s proprietary lipid-based drug delivery platform.
  • Develop scalable synthetic processes that could eventually lead to commercial use in LNP and targeted LNP formulation.
  • Characterize, problem solve and interpret analytical data obtained from instrumentation such as HPLC, LC-MS, NMR etc.
  • Maintain Chemistry laboratory and inventories in accordance with good laboratory procedures.
  • Communicate regularly with supervisor and peers on research findings and propose suggestions for next steps.
  • Maintain a current knowledge of latest technology and scientific trends.
  • Perform other duties as needed.

Required Qualifications

  • A minimum of a Ph.D. in organic, polymer or lipid chemistry from an accredited University.
  • A minimum of 1 year of post-doctoral experience in academia or industry. Experience in a GMP environment is a plus.
  • Must have proven track record of scientific accomplishments either in the form of publications or patents.
  • Excellent communication and problem-solving skills
  • A sense of humility and an eagerness to continue to learn and contribute to a supportive team

Requirements

  • A minimum of a Ph.D. in organic, polymer or lipid chemistry from an accredited University.
  • A minimum of 1 year of post-doctoral experience in academia or industry.
  • Experience in a GMP environment is a plus.
  • Must have proven track record of scientific accomplishments either in the form of publications or patents.
  • Excellent communication and problem-solving skills
  • A sense of humility and an eagerness to continue to learn and contribute to a supportive team

Benefits

  • Medical Insurance
  • Vision Insurance
  • Dental Insurance
  • 401(k) Retirement Plan
  • Retirement Savings Plan
  • Company Retirement Plan Match
  • Short-Term Disability Insurance
  • Long-Term Disability Insurance
  • Paid Parental Leave
  • Paid Time Off
  • Paid Company Holidays
  • Paid Sick Leave
  • Compassionate Leave
  • Jury Duty Leave
  • Floating Holidays
  • Personal Days
  • Free Colleague Meals
  • Onsite Massages
  • Onsite Gym
  • Flexible Spending Account
  • Health Savings Account
  • Life and AD&D Insurance
  • Legal Assistance
  • Supplemental Insurance Plans
  • Commuter Benefits
  • Well-Being Initiatives
  • Peer-to-Peer Recognition Programs

Company overview

GenScript ProBio is a global contract development and manufacturing organization (CDMO) specializing in advanced therapies, operating as a subsidiary of GenScript Biotech Corporation. Founded in 2020 and headquartered in Pennington, New Jersey, the company provides end-to-end CDMO services from drug discovery to commercialization, with a particular focus on cell and gene therapies, biologics, and recombinant protein drugs. ProBio's comprehensive service portfolio includes plasmid DNA manufacturing, viral vector production (AAV and lentiviral platforms), antibody discovery, mRNA vaccines, and antibody-drug conjugates. The company operates state-of-the-art GMP facilities, including a flagship 128,000 sq ft Cell and Gene Therapy Center of Excellence in Hopewell, New Jersey, which supports clinical-stage development and manufacturing. With expertise spanning CGT, antibody development, and protein therapeutics, ProBio aims to accelerate drug development timelines for biopharmaceutical innovators through proactive strategies, professional solutions, and efficient processes. The company has supported over 135 IND programs globally and employs advanced technologies to streamline therapeutic development from concept to clinic.

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