New 
Research Associate II
 Spectraforce Technologies | |
 United States, Massachusetts, Waltham | |
 Apr 02, 2026 | |
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Research Associate II Waltham, MA, 02145 12 months Hours: 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. | |