Parenteral MS&T Intern/Co-Op
Confirmed live in the last 24 hours
Bristol-Myers Squibb

10,001+ employees

Develops therapies for serious diseases using translational medicine.
Company Overview
Bristol Myers Squibb stands out as a leader in the biopharma industry, with a diverse team of experts dedicated to transforming patients' lives through scientific advancements in areas like oncology, hematology, immunology, cardiovascular disease, and fibrosis. The company's commitment to health equity, demonstrated through the Bristol Myers Squibb Foundation, and its use of translational medicine and data analytics to personalize patient care, set it apart from competitors. The culture at BMS encourages growth and offers opportunities that are unique in scale and scope, making it an inspiring place to work.
Data & Analytics

Company Stage


Total Funding





Lawrence Township, New Jersey

Growth & Insights

6 month growth


1 year growth


2 year growth

Franklin Township, NJ, USA
Experience Level
  • Candidates must be a US citizen, have a lawful permanent resident of the US or otherwise authorized to work in the US without requiring sponsorship now or in the future
  • Candidates must be currently enrolled in an accredited college/university seeking an undergraduate degree, Master or PhD degree in science or engineering (eg, pharmaceutical sciences, pharmacy, and chemical engineering)
  • Hands-on experience in a laboratory setting where process development/optimization studies will take place
  • Able to design and execute scientifically sound, hypothesis driven experiments
  • Capable to perform statistical analysis of experimental data in support of hypothesis driven experiments
  • Skilled in writing/reviewing study plans and scientific reports
  • Excellent communication skills, both written and verbal are required
  • Ability to work independently and effectively collaborate with cross-functional teams
  • Must be eligible to work full-time, 40 hours per week, during intern (Jun 2024 - Aug 2024) /co-op (June 2024 - Dec 2024) program
  • Characterization, optimization and troubleshooting product and manufacturing processes of parenteral dosage forms
  • Collaboration with R&D and manufacturing sites to design and execute experiments to support product robustness, new technology implementation, and/or manufacturing investigations
  • Serve as technical resource to other functions, providing expertise on the product and its process
  • Provide assistance to sites globally to resolve significant quality events and manage complex change controls