Intern, Manufacturing, Science and Technology

Bristol Myers Squibb • Indianapolis, IN

3d • $23 - $42

About The Position

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. 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. RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals. Summary The MS&T Intern will participate and support the different teams within the MS&T department including process engineering, validation, and deviation activities. The intern will support the development, optimization, and validation of manufacturing processes to ensure compliance with regulatory standards and the production of high-quality radiopharmaceuticals. The full-time internship will take place June - August 2026.

Requirements

• Current enrollment in a Bachelor’s or Master’s degree program in engineering, science, or a related field.
• Basic understanding of pharmaceutical manufacturing processes, validation principles and regulatory requirements is preferred
• Familiarity with process equipment and validation methodologies is a plus
• Prior internship or coursework in pharmaceutical manufacturing, process engineering, or quality assurance is desirable but not required
• Eagerness to learn and adapt in a dynamic, regulated environment
• Strong organizational skills and ability to manage multiple tasks
• Commitment to maintaining high standards of safety, quality, and compliance.
• Strong analytical and problem-solving skills with attention to detail
• Proficiency in Microsoft Office
• Ability to work independently and collaboratively in a team-oriented environment
• Excellent written and verbal communication skills
• 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.
• Ability to climb ladders and lift up to 50 lbs.
• This is a position that requires working in a GMP cleanroom environment, wearing protective clothing, and handling of radioactive materials.

Responsibilities

• Assist in the development and execution of validation protocols for equipment, facilities, utilities, and processes used at the site.
• Support process engineering activities including troubleshooting, process optimization, and data analysis to improve manufacturing efficiency and product quality
• Collect, analyze, and document data from various types of validation studies
• Collaborate with cross-functional teams to ensure compliance with GMP and regulatory requirements
• Participate in risk assessments and failure mode effect analysis (FMEA) to identify risks and implement corrective and preventative actions
• Assist in drafting Standard Operating Procedures (SOPs), batch records, technical documents, and other document types utilized at the site.
• Contribute to continuous improvement initiatives by identifying opportunities to enhance process efficiency, reduce costs, or improve product quality.
• Maintain accurate and detailed documentation for all activities in compliance with regulatory standards.

Benefits

• Health Coverage: Medical, pharmacy, dental, and vision care.
• Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
• Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
• Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

What This Job Offers

• Job Type: Full-time
• Career Level: Intern
• Number of Employees: 5,001-10,000 employees