Summer Intern PhD Student - Drug Product Development Sterile Formulation
Listed on 2026-10-18
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Pharmaceutical
Pharmaceutical Science/ Research -
Research/Development
Pharmaceutical Science/ Research
At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits.
This is work that transforms the lives of patients, and the careers of those who do it. Drug Product Development works with colleagues throughout the entire pharmaceutical development process, from discovery to commercial launch and beyond, to deliver drug products of biologics and small molecules, including sterile formulations and novel drug delivery technologies. We are looking for candidates who are proven team players;
appreciate the challenge of pursuing unique scientific discovery in an emerging field; and who demonstrate solid operational, interpersonal, project management and collaborative skills. We believe this starts with our summer intern program. Summer interns will work with mentors for ~10 weeks on a guided research project related to sterile formulation development and novel drug delivery technologies for both biologics and small molecules, spanning liquid, lyophilized, and other advanced delivery platforms.
This position integrates wet-lab and dry-lab functions: interns will conduct feasibility experiments with formulation and processing technologies, supporting formulation development, formulation screening, stability assessment, physicochemical and biophysical characterization of critical quality attributes, and process optimization. The project may also involve biopharmaceutical investigation of biologics, exploring structure-function relationships, degradation pathways, and stability‑indicating strategies to inform formulation design and enable robust, patient‑friendly drug products.
The program is organized to ensure that interns gain valuable industry and functional experience, work on challenging assignments, learn about BMS and meet diverse company representatives.
- An orientation, including an overview of company structure, products and brands
- An introduction to the GPS and PD organizations
- Exposure to senior management and business leaders
- Hands‑on training and working experiences in pharmaceutical manufacturing process areas and testing laboratories
- Formal presentation at the end of your internship
- A mentor program
- Formal review and feedback sessions
Program Dates:
Monday June 7, 2027 - Friday, August 13, 2027. Applications are currently being accepted and may be selected on a rolling basis. Those selected will be notified no later than February 2027. Position is in New Brunswick, NJ.
- Candidates must be currently enrolled in an accredited university program seeking a PhD degree in Pharmaceutical Science, Pharmaceutical Chemistry, Biotechnology, Chemical or Biomedical Engineering, or a related discipline
- Candidates are expected to graduate between Fall 2027 and 2028
- Must include GPA on resume for consideration (program requires GPA of 3.0 or greater)
- All candidates must be authorized to work in the US both at the time of hire and for the duration of their employment
- Please note that immigration or visa sponsorship is not available for this position
- Must have strong verbal, written, and interpersonal skills and be able to work in a team environment
- Ability to solve problems independently with minimal supervision
Hands‑on lab experience is expected - Sound knowledge and understanding of the fundamental principles of pharmaceutical science, physical pharmacy, chemistry, stability,…
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