Working with Us

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

The intern will be responsible for conducting lab experiments and paper evaluations of excipient sources for oral solid dosage products that are manufactured in internal sites and external contractors. The intern will work closely with the Pharmaceutical Development (PD) team to evaluate specifications, raw material attributes, and potential impact to the drug product process.

Key Responsibilities:

• Conduct lab experiments to evaluate the quality and performance of excipient sources for oral solid dosage products.
• Evaluate paper documentation related to excipient sources and assess their suitability for use in drug product manufacturing.
• Collaborate with the PD team to identify potential risks and impacts of excipient sources on the drug product process.
• Analyze data and prepare reports to communicate findings and recommendations to the PD team.
• Participate in team meetings and contribute to ongoing projects related to excipient sourcing and drug product development.

Qualifications:

• Currently enrolled in a Bachelor’s or Master’s degree program in Chemistry, Pharmaceutical Sciences, or related field.
• Familiar with pharmaceutical manufacturing processes and quality control.
• Experience with laboratory techniques and equipment.
• Excellent analytical and problem-solving skills.
• Strong attention to detail and ability to work independently.
• Effective communication and teamwork skills.
• Candidates must be US citizens, be lawful permanent residents of the US, or otherwise authorized to work in the US without requiring sponsorship now or in the future.

This internship provides an opportunity to gain hands-on experience in the pharmaceutical industry and contribute to the development of safe and effective drug products. The intern will work closely with experienced professionals and have the opportunity to learn about the drug development process from start to finish.

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers

With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Bristol Myers Squibb is a leading global biopharma company focused on discovering, developing and delivering innovative medicines for patients with serious diseases in areas including oncology, hematology, immunology, cardiovascular, fibrosis and neuroscience. Our employees work every day to transform patients’ lives through science.