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Associate Scientist

BioPharma Consulting JAD Group
Cambridge, MA Contractor
POSTED ON 1/26/2025
AVAILABLE BEFORE 7/22/2025
Summary:

Summary:

BioPharma Consulting JAD Group is looking for a motivated Associate Scientist to join our dynamic team. The successful candidate will be a part of the CMC - DS Process Development Group, responsible for the process development to incorporate novel chemistries into our manufacturing platform.

Key Responsibilities:

  • Support oligonucleotide synthesis method development, optimization and scale-up
  • Support downstream processing method development
  • Execution of in-process analytical testing
  • Working with research and process scientists to develop robust processes for novel chemistries
  • Conduct laboratory experiments and research to support ongoing projects, following established protocols and methodologies
  • Compile and analyze experimental data, generating reports and summaries for senior scientists and project teams
  • Develop and optimize assay methods, providing technical insights for process improvements and innovative approaches
  • Maintain accurate and detailed laboratory records, ensuring compliance with GLP and GMP standards
  • Collaborate with cross-functional teams to achieve project milestones and objectives
  • Contribute to the preparation of scientific presentations, documentation, and technical reports
  • Participate in the maintenance of laboratory equipment and inventory management, ensuring a safe and efficient laboratory environment


Skills:

  • Basic understanding of analytical techniques (pH, osmolality, conductivity measurement, HPLC, LC-MS etc.)
  • Knowledge of oligonucleotide manufacture process including phosphoramidite chemistry, chromatography, ultrafiltration etc.
  • Record-keeping and excellent laboratory documentation practice
  • Ability to maintain a safe, clean, and orderly laboratory work environment
  • Good communication skills.


Requirements

Qualifications:

  • Bachelor's degree in Chemistry or Chemical Engineering with 0-3 years of lab experience


Preferred Qualifications:

  • Familiarity with laboratory techniques such as PCR, chromatography, and electrophoresis
  • Experience in data analysis software and scientific reporting tools
  • Knowledge of GLP/GMP regulations and practices
  • Basic understanding of biopharmaceutical processes and drug development lifecycle
  • Hands-on experience with assay development and optimization is a plus

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