Senior Researcher

Mindlance; Waltham (MA); On-site; USD 50,000 - 70,000; Full time

Job summary

A biotechnology company in Waltham, MA is seeking a motivated Research Associate to perform GMP and non-GMP testing for AAV and LNP mRNA programs. The ideal candidate should have a background in Analytical Chemistry or Biochemistry, with hands-on experience in analytical techniques like Liquid Chromatography and Mass Photometry. Responsibilities include supporting method development and ensuring compliance with regulatory standards. This full-time role offers an excellent opportunity for growth in a dynamic laboratory environment.

Qualifications

• 1–3 years of relevant biotechnology or pharmaceutical industry experience for Bachelor's; 0–1 year for Master's.
• Familiarity with regulatory requirements for genomic medicine development.
• Previous experience in a GMP environment.

Responsibilities

• Independently perform GMP and non-GMP Quality Control testing of AAV and LNP mRNA samples.
• Document all testing activities and results accurately.
• Support analytical method development, qualification, and transfer.

Skills

Hands-on analytical experience

Understanding of biomolecular chemistry

Analytical troubleshooting

Education

Bachelor's degree in Analytical Chemistry, Biochemistry, or a related discipline

Master's degree

Tools

Liquid Chromatography

Capillary Electrophoresis

Mass Photometry

Empower 3 software

Job description

Duration: 12+month with potential extension. Site: Waltham, MA

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.

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.

EEO:

“Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”