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Bristol Myers Squibbposted about 1 month ago
Intern
Hybrid • New Brunswick, NJ
Chemical Manufacturing
Resume Match Score

About the position

The Forensic Scientist Co-Op will work with Subject Matter Experts in Forensics and Innovative Technologies (FIT) group. The student will learn to operate several state-of-the art analytical instruments such as, SEM/EDS, digital microscope, FT-IR, Raman, Near-Infrared, UV/VIS, MS, and other micro-spectrometers and apply them for forensics testing to support manufacturing, patient complaints, and counterfeit product investigations. This is a 6-Month Opportunity from July 7th - December 13th, 2025 in New Brunswick, NJ.

Responsibilities

  • Support manufacturing investigations through characterization and identification of extraneous/foreign matter samples using relevant analytical techniques (mid-IR, Raman, SEM/EDS, microscopy).
  • Support the investigation of product quality complaints through analysis of returned samples.
  • Perform suspect product authentication using NIR, mid-IR and Raman spectroscopy.
  • Develop spectral database using existing and by acquiring spectra (FT-IR and Raman) using KnowItAll software.
  • Perform routine calibration and maintenance activities for analytical instruments in a GMP laboratory setting.
  • Document all experiments in laboratory notebooks to GMP standards.
  • Author and issue investigation reports relating to analytical support provided.

Requirements

  • CURRENTLY ENROLLED FALL 2025 AS a Senior pursuing a BS or pursuing an MS in Chemistry, Physics, Biology, Biochemistry or Engineering. Minimum GPA 3.0.
  • All candidates must be authorized to work in the US at the time of hire. Please note that immigration or visa sponsorship is not available for this position.
  • Experience working with spectroscopic and chromatographic techniques such as UV, mid-IR, NIR, Raman, MS, GC and HPLC is highly desirable.
  • Proficient written and oral communication skills; attention to detail; team oriented and ability to multi-task.
  • Proficient with computers and experience with typical office and scientific/instrument software applications.
  • Knowledge of global pharmaceutical regulatory requirements is highly desirable.
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