Senior Research Associate

About The Role

We are seeking a highly motivated Senior Research Associate to support the development, optimization, and scale-up of mRNA manufacturing processes. This role will focus on in vitro transcription (IVT), downstream purification, and analytical testing to support process development activities and technology transfer initiatives.

We are seeking a highly motivated Senior Research Associate to support the development, optimization, and scale-up of mRNA manufacturing processes. This role will focus on in vitro transcription (IVT), downstream purification, and analytical testing to support process development activities and technology transfer initiatives. The ideal candidate will have hands‑on experience with mRNA production processes, strong laboratory skills, and a passion for advancing innovative RNA-based therapies.

This position offers the opportunity to work in a collaborative, fast‑paced environment while contributing to the development of cutting‑edge biopharmaceutical products.

• Perform and support RNA manufacturing processes at small and intermediate scale using stirred tank and Wave reactor systems.
• Execute and support in vitro transcription (IVT) reactions and downstream purification processes.
• Troubleshoot, optimize, and scale up IVT and purification processes to improve performance and manufacturing readiness.
• Support process development, technology transfer, and scale-up activities for RNA and other drug substance manufacturing processes.
• Perform analytical testing to evaluate RNA purity, integrity, and concentration using techniques such as Fragment Analyzer and Nano Drop.
• Operate and maintain laboratory equipment used in process development and analytical testing.
• Document experimental activities, results, and observations in accordance with Good Documentation Practices (GDP).
• Follow Good Laboratory Practices (GLP), laboratory safety procedures, and applicable biosafety requirements.
• Collaborate with cross‑functional teams to support development, manufacturing, and client‑driven projects.
• Prepare technical summaries and effectively communicate results and recommendations.
• Perform other duties and projects as assigned.

• Bachelor's degree in Pharmaceutical Sciences, Biotechnology, Biochemistry, Chemical Engineering, Biomedical Engineering, or a related scientific discipline with 1 to 5 years of relevant industry experience; or a Master's degree with relevant hands‑on experience.
• Experience supporting mRNA, RNA, or drug substance process development activities.
• Hands‑on experience with AKTA chromatography systems and purification process development.
• Experience with Tangential Flow Filtration (TFF), process optimization, scale‑up, and/or technology transfer activities.
• Experience performing analytical characterization using techniques such as:
  • Fragment Analyzer or Capillary Electrophoresis (CE)
  • Bioanalyzer or gel electrophoresis
  • UV spectroscopy
  • Nano Drop analysis
• Knowledge of process development principles within the pharmaceutical or biotechnology industry.
• Familiarity with laboratory safety requirements, including biosafety practices and BSL requirements.
• Strong attention to detail and ability to maintain accurate documentation.
• Excellent written and verbal communication skills.
• Ability to work independently while contributing effectively within a team environment.

• Experience working with circular RNA (circRNA).
• Experience supporting GMP manufacturing environments and technology transfer projects.
• Knowledge of RNA-based therapeutic manufacturing processes.

• Frequent standing, sitting, use of hands, reaching, and communication with team members.
• Occasional walking,…