S
Not Specified Permanent

Cambridge, Massachusetts · USA job

Scientist, Analytical Development and Quality Control

Seres Therapeutics

Cambridge, Massachusetts

Job description

Overview

In this role, you will strengthen and advance our analytical platform for nucleic acid therapeutics and LNP delivery systems. You will work closely with a cross-functional, fast-paced team to develop and qualify assays, generate robust data, and support product release and stability characterization. You'll contribute hands-on benchwork and guide junior staff, shaping our quality and analytical capabilities in a dynamic entrepreneurial environment. This position offers meaningful impact in enabling novel gene therapy solutions at Serif Biomedicines.

Compensation / Benefits
  • healthcare coverage
  • annual incentive program
  • retirement benefits
  • broad range of other benefits
Responsibilities
  • Drive platform development and shape analytical capabilities
  • Perform bench work to achieve platform goals with tenacity
  • Set up, maintain, and optimize a system for efficient sample testing and data delivery
  • Ensure data robustness through lineage tracking of historical data
  • Conduct method development for nucleic acid cargo and LNP product release, stability, and characterization
  • Lead experimental studies to optimize specificity, sensitivity, precision, accuracy, and/or linearity of analytical methods
  • Analyze, troubleshoot, and clearly communicate experimental findings
  • Troubleshoot assay development and instrument operation issues
  • Run assays on samples from platform development studies
  • Maintain inventory of nucleic acid cargo and materials for development and formulation
  • Document activities with detailed protocols/reports in Benchling
  • Write and revise SOPs; train team on new assays
  • Present results to internal teams
  • Support general lab operations
  • Work independently and collaboratively in a multidisciplinary team environment
Key requirements
  • Degree in Chemistry, Biochemical Engineering, Biochemistry, Molecular Biology, Chemical Engineering, Biotechnology or related field
  • B.S. with 10+ years, M.S. with 8+ years, Ph.D. with 0+ years of relevant industry experience
  • Technical expertise in HPLC separations and plate-based assays (ELISA, qPCR/dPCR, residual protein)
  • Experience with HPLC methods for mRNA/DNA cargo and nanoparticle delivery (LNPs, liposomes) is highly desired
  • Proven ability to independently design, execute, and troubleshoot complex experiments
  • Experience mentoring or training junior staff is desired
  • Strong communication and organization skills; familiarity with Benchling, MS Office, JMP, GraphPad, Empower, Chromeleon
  • Attention to detail, meticulous record keeping and personal organization
  • Ability to analyze, compile, and present data in oral presentations and technical reports
  • Strong technical writing skills for SOPs, protocols, and reports
  • mentoring
  • clear communication
  • attention to detail
  • HPLC separations
  • ELISA
  • qPCR/dPCR

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