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Finish Line Staffing Services
Published
February 7, 2025
Location
Cambridge, MA
Category
Default  
Job Type

Description

Overview
The successful candidate will be a part of the Process Chemistry group, responsible for the process development and in-house non-GMP manufacture of modified oligonucleotides and siRNAs.

Summary of Key Responsibilities

  • Support non-GMP oligonucleotide production on a tight timeline
  • Support purification method development, optimization, and scale-up
  • Execute non-GMP oligonucleotide purifications
  • Perform downstream processing of purified material
  • Conduct in-process analytical tests
  • Participate in creating and reviewing SOPs and batch records
  • Support campaign activities across other unit operations as needed

Qualifications

  • Bachelor’s degree in Chemistry with 1-3 years of laboratory experience, preferably in an industrial setting
  • Basic understanding of analytical techniques such as pH, osmolality, conductivity measurement, HPLC, and LC-MS; hands-on experience is preferred
  • Knowledge of oligonucleotide manufacturing processes, including phosphoramidite chemistry, chromatography, and ultrafiltration, is a plus
  • Experience in record-keeping and strong laboratory documentation practices
  • Commitment to high laboratory and scientific standards; ability to maintain a safe, clean, and orderly laboratory work environment; assist in routine lab and equipment maintenance
  • Strong communication skills are essential
  • A responsible and proactive individual who can work effectively as part of a team in a highly dynamic environment with aggressive timelines

 

Apply
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