Technology Management Monoclonal Antibody (mAb) Intern

Join a Legacy of Innovation 125 Years and Counting!

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 18,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for cardiovascular diseases, under the Group’s 2025 Vision to become a “Global Pharma Innovator with Competitive Advantage in Oncology,” Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.  

We are currently seeking a Technology Management Monoclonal Antibody (mAb) Intern for Summer 2026. This full-time position works for approximately 37.5 hours per week.
 

Responsibilities:

As CMC Technology Management, we support every step of CMC strategy, manufacturing, submission and health authority engagement through all phases of the product lifecycle: Early Development, Tech Transfer, Process Performance Qualification (PPQ) through Commercialization. Our group is seeking a summer intern interested in enhancing core knowledge and applied critical thinking skills in Technology Management of monoclonal antibodies to develop and commercialize Daiichi Sankyo’s ADCs pipeline projects. This opportunity will expose the intern to various areas of the department and provide beneficial experience and understanding of CMC principles, strategies, and processes:

• Understand regulatory compliance/requirements of manufacturing clinical and commercialization products.
• Support Tech Transfer of Biologics Manufacturing processes within our company’s internal and external manufacturing network and Potential involvement with all phases of project management
• Work with operations and quality groups to maintain products at a high level of performance/compliance
• Collaborate with cross-functional teams internally and externally to improve and/or optimize CMC related business processes
• Review completeness of documentation to support IND/BLA/MAA submissions
• Understand manufacturing changes to ensure compliance with appropriate change control systems/process and support regulatory filing strategy (PAS, CBE, Annual Reports, etc.)
 

Qualifications:

• Qualified candidates must currently be enrolled in an accredited undergraduate program with a concentration in Chemical, Biochemical, Biomedical or other related Engineering disciplines, Regulatory or pharmaceutical science, or other related fields in science and technology (Chemistry, Biology, Microbiology, Operations Research, Industrial Engineering, etc.) or related field.
• Prior experience in a corporate business environment is preferred; experience in the pharmaceutical industry is a plus.
• Candidates must have excellent academic achievement and analytical thinking ability.
• Candidates should have knowledge of current Good Manufacturing Practices (cGMPs), data analytics experience.
• Candidates should have pharmaceutical science and manufacturing process unit operation knowledge.
• Candidates should have experience writing, editing, and reviewing scientific publications and content.
• Candidates must have good organizational skills.
• Candidates must have superior communication and interpersonal skills.

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer.  All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.  

Salary Range:

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