2027 Future Talent Program – Regulatory Chemistry, Manufacturing and Controls – Intern
About The Position
The Future Talent Program features internships that last up to 12 weeks and will include one or more projects. These opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the right company for your long-term goals. Join our Company's Research Laboratories for an exciting Summer 2027 internship opportunity within the Global Regulatory Chemistry, Manufacturing and Controls (CMC) organization. As a Regulatory CMC intern, you will have the opportunity to contribute to the development and lifecycle management of innovative products that impact patients worldwide. This internship is designed for students interested in regulatory affairs and pharmaceutical development, with opportunities spanning biologics, small molecules, vaccines, and drug-device combination products. Students interested in advancing regulatory innovation through digital solutions, automation, artificial intelligence, and process improvement initiatives are also encouraged to apply. Through meaningful project work, you will gain hands-on experience supporting Regulatory CMC strategy, global submissions, health authority interactions, and regulatory compliance activities. As an intern, you will gain exposure to a diverse range of functions across our Company's research, development, manufacturing, and regulatory organizations while developing a strong foundation in Regulatory CMC principles and practices. Experiences may include supporting the development of regulatory submission content, learning about the manufacture and testing of drug substances and drug products, understanding regulatory requirements for investigational and commercial products, contributing to post-approval regulatory strategies, and participating in cross-functional collaborations that support product development and supply continuity.
Requirements
- Currently pursuing a minimum of a bachelor’s degree in regulatory science, pharmaceutical science, pharmacy, chemistry, biomedical or other engineering disciplines, or other related fields in science and technology
- Have completed at least (2) years of study undergraduate OR (1) year of study graduate by June 2027
- Available to work full-time for up to (12) consecutive weeks beginning in May or June 2027
- Superior communication and interpersonal skills
- Excellent academic achievement and analytical thinking ability
- Good organizational skills
Nice To Haves
- GPA of 3.5 and above
- Proficiency in Microsoft Office applications
- Experience writing, editing, and reviewing scientific publications and content
Responsibilities
- Contribute to the development and lifecycle management of innovative products.
- Support Regulatory CMC strategy, global submissions, health authority interactions, and regulatory compliance activities.
- Support the development of regulatory submission content.
- Learn about the manufacture and testing of drug substances and drug products.
- Understand regulatory requirements for investigational and commercial products.
- Contribute to post-approval regulatory strategies.
- Participate in cross-functional collaborations that support product development and supply continuity.
Benefits
- Equal Employment Opportunity Employer
- Affirmative action requirements for protected veterans and individuals with disabilities
- Accommodation during the application or hiring process
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What This Job Offers
Job Type
Full-time
Career Level
Intern
