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Research Associate - Analytics, Cell & Gene Therapies

LandmarkbioWatertown, MA

Data and analyticsEntry levelFull time1+ yrs
Source-verified: read directly from this employer's own lever job board, not a repost.HybridPosted (2 months ago)Last verified (today)

At a glance

Location
Watertown, MA
Workplace
Hybrid
Pay
Not published by the employer
Employment type
Full time
Experience
1+ years
Education
Master (required)
Job family
Data and analytics
Seniority
Entry level
Posted by employer
6 August 2026
Last verified open
23 October 2026
Region and country
MA, US
Team
Science and Technology Operations
Listed via
Lever

What the employer wrote

The Analytics department at Landmark Bio/Artis BioSolutions supports a growing portfolio of advanced cell and gene therapies (CGT), including CAR-T, iPSC, AAV, LVV and synthetic DNA products. We are immediately hiring two driven Research Associates. In this role, you will develop, qualify, and execute methods for CGT product release and characterization. You will also collaborate with analytical, process, engineering, manufacturing, and compliance teams. This is a great opportunity to learn from mentors while managing analytical tasks in a fast-paced environment to test product safety, identity, potency, purity, and quality including compendial applications. These hands-on, lab-based roles require working on-site at Landmark Bio/Artis BioSolutions in Watertown, MA, with flexible schedules to support technical operations.

Responsibilities • PCR Testing:  Develop, optimize, and transfer PCR methods (qPCR, dPCR, ddPCR) for molecular testing.

• Cell & Proteomic Assays:  Support automated cell counters, cell-based cytotoxicity assays, flow cytometry, and ELISA-based testing.

• Extracellular Vesicles and Particle Analysis:  Nanoparticle Tracking, Light Scattering, and Nano Flow Cytometry

• Biophysical Analysis:  Run and troubleshoot UHPLC methods (Reverse Phase, Size Exclusion) for purity and residual analysis.

• Data Documentation:  Maintain precise electronic lab notebooks and draft GMP technical protocols or reports.

• Lab Maintenance:  Calibrate lab instrumentation, troubleshoot performance errors and handle routine equipment upkeep.

• Safety & Compliance:  Follow all environmental health and safety standards while meeting regulatory guidelines.

 

Qualifications • Education:  Bachelor’s or Master’s degree in Biology, Biotechnology, Molecular Biology, or a related field.

• Experience:  Minimum of 1+ years of work experience, preferably in a cGMP biotechnology manufacturing setting or equivalent higher degree academic research.

• Skills:  Experience with cell/gene therapy, analytical problem-solving, and strong oral and written communication.

• Work Authorization:  Must possess valid, unrestricted work authorization and be available to start immediately.

To apply, submit a resume and a cover letter that specifically details your: Unrestricted work authorization status Hands-on experience in one or more relevant lab techniques (PCR, UHPLC, Cell-based or Molecular) Familiarity with cGMP and cell and gene therapy regulatory frameworks Landmark Bio/Artis BioSolutions is an Equal Opportunity, Affirmative Action employer. Minorities, women, veterans, and individuals with disabilities are encouraged to apply.

Where this record came from

Read from Landmarkbio's own Lever job board on , and last confirmed still open on . The employer published it on 6 August 2026. Jobsearch.ing did not write, edit or rank this posting, and does not vet the employer. View the original posting.

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