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Contract Research Associate, Analytical Development

Orbital Therapeutics
Cambridge, MA Full Time
POSTED ON 3/7/2025
AVAILABLE BEFORE 6/6/2025

Orbital Therapeutics is on a mission to enhance global health by unleashing the full potential of RNA medicines to treat human disease in ways that were not previously possible.

With a combination of deep and diverse expertise, accomplished leadership, and a comprehensive range of state-of-the-art technologies, we are determined to elevate the possibilities of RNA medicines by leading the future. We are building a portfolio of innovative RNA medicines across three areas – immunomodulation for autoimmune disease and oncology, next-generation vaccines, and protein therapeutics. Launch into broader territory at Orbital - join our team as we embody rigorous science, welcome big ideas, and embrace the great possibilities of RNA medicines.

Position Summary

Orbital Therapeutics is seeking a skilled Research Associate with experience in chromatography to join the Analytical Development team to support testing of novel RNA therapeutics. The successful candidate will help execute and analyze routine testing and assist in developing and onboarding new physicochemical assays.

Responsibilities :

  • Perform stability testing for RNA related testing samples and formulated drug product samples, including compendial methods along with biophysical testing such as particle size, LNP encapsulation, etc.
  • Support routine analytical testing for research program needs, such as with chromatography-based methods (HPLC) and / or biochemical assays such as ELISA assays.
  • Work with other team members to onboard new and / or improve existing analytical methods.
  • Partner collaboratively with internal teams (process development, formulation development, research, preclinical manufacturing) to meet analytical development and routine testing needs.
  • Document and communicate results to team members.
  • Managing external stability testing results with CDMOs, if needed.
  • Perform stability data trending, as needed.

Qualifications :

  • B.S. or M.S. in Analytical Chemistry, Biochemistry or related discipline, with 2 years of relevant experience.
  • Past experience with quality control, preferably with a focus on stability, is required.
  • Hands-on experience analyzing chemical or biological samples using chromatography (HPLC / UPLC) in various modes (reversed phase, ion exchange, etc.) and associated detection methods is required.
  • Good understanding with cGMP, GDP and GLP regulations and guidelines.
  • General experience in data analysis and statistical evaluation / data trending.
  • Experience with biochemical assays such as ELISA, Western blot, etc. is preferred.
  • Ability to work independently as well as in a team.
  • Detail-oriented in assay execution and documentation.
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