More jobs:
Senior Researcher
Job in
Waltham, Middlesex County, Massachusetts, 02254, USA
Listed on 2026-08-22
Listing for:
Mindlance
Full Time
position Listed on 2026-08-22
Job specializations:
-
Research/Development
Pharmaceutical Science/ Research -
Quality Assurance - QA/QC
Job Description & How to Apply Below
Duration: 12+month with potential extension. Site:
Waltham, MA
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.
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.
- 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.
- 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.
EEO:
“Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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