Intern, Manufacturing, Science and Technology

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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.

Job Responsibilities

Essential duties and responsibilities include the following.  Other duties may be assigned.

·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.

Education and Experience

·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

Skills and Qualifications

·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