Senior Analytical Scientist — LNP & Nucleic Acids

Seawolf Therapeutics, Inc.

San Diego (CA)

On-site

USD 60,000 - 95,000

Full time

10 days ago

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Benefits offered by this job

medical
dental
vision
life insurance
401K
stock options
bonus

Job summary

Seawolf Therapeutics, Inc. in San Diego, CA is seeking a Research Associate/Sr. Research Associate to join our Analytical Development team.

This on-site role involves 80% lab-based work developing methodologies to analyze nucleic acid-based therapeutics, with a focus on HPLC- and CE-based analyses of LNP drug product formulations. The ideal candidate has a BS/MS in a related field and at least 2 years of industry experience, strong documentation habits, and the ability to collaborate across a

Qualifications

  • BS/MS in chemistry, chemical engineering, bioengineering or related field with at least 2 years of relevant industry experience.
  • Strong documentation and data integrity practices.

Responsibilities

  • Assist in the development of new analytical methods for the characterization of lipids, nucleic acids, and nanoparticle formulations.
  • Perform routine analytical testing of in-process and drug product LNP formulations to assess concentration, identity, purity, and integrity.
  • Maintain meticulous documentation of all experimental data, procedures, and protocols.
  • Maintain organized storage and inventory of supplies and materials.
  • Collaborate with a team of scientists to creatively solve problems and drive innovation.
  • Maintain high standards for scientific integrity and accountability.
  • Communicate across departments and support project teams.

Skills

Analytical thinking
Troubleshooting
Data analysis
Scientific communication
Team collaboration
Startup adaptability

Education

BS/MS in chemistry or related field

Tools

HPLC
CE
Microsoft Excel
Automation tools

Job description

Seawolf Therapeutics, Inc. in San Diego, CA is seeking a Research Associate/Sr. Research Associate to join our Analytical Development team.

This on-site role involves 80% lab-based work developing methodologies to analyze nucleic acid-based therapeutics, with a focus on HPLC- and CE-based analyses of LNP drug product formulations. The ideal candidate has a BS/MS in a related field and at least 2 years of industry experience, strong documentation habits, and the ability to collaborate across a

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