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BeOne Medicines

Intern – Regulatory Affairs, CMC

BeOne Medicines

Regulatory Affairs Intern supporting regulatory projects in a Biotech company. Gaining hands-on experience and understanding of drug development process and regulatory requirements.

Posted 5/7/2026internshipRemote • 🇺🇸 United StatesEntry LevelWebsite

About the role

Key responsibilities & impact
  • Be exposed to the broad scope of global Regulatory Affairs and specifically CMC Regulatory Affairs and the role’s contribution to drug development and patients’ access to medicines.
  • Learn about the role of global Health Authorities in the drug development process.
  • Gain hands-on experience in preparing regulatory documents for submission to global health authorities.
  • Acquire knowledge about the differences in regulatory requirements across regions.
  • Experience CMC technical product development and manufacturing functions in relation to regulatory affairs.
  • Responsible for maintaining accurate CMC information in the BeOne Regulatory Information Management system.
  • Data remediation.
  • Create and maintain CMC Submission Content.
  • Upload HA Correspondence/HA Questions/Commitments.
  • Maintain internal Regulatory CMC trackers.
  • Contribute to Reg CMC process improvements.
  • Support the drafting of CTD CMC sections to ensure on-time and high-quality global applications for direct submission to Health Authorities as needed.
  • Provide support to Reg CMC team or hiring manager with Regulatory submissions and other tasks as needed.

Requirements

What you’ll need
  • Active enrollment (Graduate or Ph.D.) in an accredited college or university pursuing a degree in a scientific discipline (e.g., life sciences, chemistry, biology, biotechnology, materials science, etc.) with a minimum 3.0 GPA
  • Awareness of processes for working in a regulated field preferred
  • Basic knowledge of healthcare industry and strong passion for biotech
  • Legally authorized to work in the United States without needing sponsorship for employment now or in the future
  • Ability to work independently on assignments with routine check-ins
  • Strong written and oral communication skills
  • Organized, responsible, resourceful, and detail-oriented
  • Able to work in a cross-cultural team environment with members across different time zones
  • Able to work remotely using MS TEAMS and other collaboration tools

Benefits

Comp & perks
  • Medical
  • Dental
  • Vision
  • 401(k)
  • FSA/HSA
  • Life Insurance
  • Paid Time Off
  • Wellness

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
CMC Regulatory Affairsregulatory document preparationdata remediationCTD CMC sections draftingtechnical product developmentmanufacturing functionsRegulatory CMC process improvementsRegulatory submissions
Soft Skills
strong written communicationstrong oral communicationorganizedresponsibleresourcefuldetail-orientedability to work independentlycross-cultural teamwork