Jobs

Description

Work Schedule: 9-5 EST; M-F

Position Summary

We are seeking a motivated and detail-oriented Research Associate to join our analytical team supporting AAV and LNP mRNA programs.

• This role involves independently performing GMP and non-GMP testing, supporting analytical method development, and contributing to laboratory investigations.
• The ideal candidate has hands-on analytical experience and a strong understanding of biomolecular chemistry within a regulated environment.

Key Responsibilities

• Independently perform GMP and non-GMP Quality Control testing of AAV and LNP mRNA samples using analytical techniques such as Liquid Chromatography (LC), Capillary Electrophoresis (CE), and Mass Photometry (MP).
• Document all testing activities and results accurately in compliance with internal and regulatory standards.
• Support analytical method development, qualification, and transfer for LC, CE, and MP assays.
• Assist with analytical troubleshooting and laboratory investigations to ensure testing accuracy and data integrity.
• Collaborate with cross-functional teams to contribute to continuous improvement initiatives and lab operational excellence.

Basic Qualifications

• Bachelor’s degree in Analytical Chemistry, Biochemistry, or a related discipline with 1–3 years of relevant biotechnology or pharmaceutical industry experience; or
• Master’s degree with 0–1 year of relevant experience.

Preferred Qualifications

• Practical, hands-on industry experience with LC, CE, MP platforms, and Empower 3 software.
• Familiarity with regulatory requirements for genomic medicine development, including appropriate control and testing strategies.
• Strong theoretical understanding of macromolecules (e.g., DNA, RNA, proteins) and their chemical properties.
• Previous experience working in a GMP environment with demonstrated ability to comply with all applicable GMP standards and documentation practices.