Scientist I or II - Biologics Downstream Process Development - FSP

ParexelUnited States-New Jersey-Remote, NJ
Onsite

About The Position

Parexel FSP is seeking a full-time Scientist 1 or 2 in Biologics Downstream Process Development. This role will be an employee of Parexel FSP and will be on a long-term assignment onsite at one of Parexel's clients in Rahway, NJ. The position focuses on supporting process development for biologics, involving high-throughput chromatographic purification, analytical characterization, and collaboration with various teams. Parexel FSP provides qualified technical professionals to support pharmaceutical and biopharmaceutical companies in the development and delivery of new therapies. They are committed to keeping patients at the center of their work and fostering an inclusive community.

Requirements

  • B.S./M.S. in chemical engineering, biological sciences, microbiology, structural biology, or related field
  • Scientist 1 - B.S. with 0-1 years of experience
  • Scientist 2 - B.S. with 1-2 years of experience; M.S. with 0-1 years
  • Basic understanding of biochemical/biophysical properties of proteins
  • Knowledge of analytical characterization methods for proteins, particularly HPLC or UPLC-based separations methods such as size exclusion or ion exchange chromatography
  • Strong organizational skills with the ability to multitask
  • Ability to work within a team environment
  • Rigorous documentation of data in electronic lab notebooks is a requirement

Nice To Haves

  • Knowledge or experience with lab automation tools like robotic liquid handlers such as TECAN
  • Knowledge or experience with purification unit operations (chromatography, filtration)

Responsibilities

  • Independently execute high-throughput chromatographic purification to support process development of programs at various stages in the pipeline
  • Complete analytical characterization of purified samples using HPLC/UPLC based methods
  • Perform lab scale chromatography and filtration experiments
  • Documentation of results in laboratory notebooks and contribute to technical reports
  • Collaborate with upstream and downstream process development and process analytical groups, coordinating submission schedules with multiple stakeholders
  • Contribute to a safe and compliant laboratory work environment

Benefits

  • full benefits
  • sick time
  • 401K
  • paid holidays
  • paid time off
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