4 days ago

Regulatory Affairs Summer Intern

BeOne Medicines

Hybrid
Full Time
$56,160
Hybrid

Job Overview

Job TitleRegulatory Affairs Summer Intern
Job TypeFull Time
CategoryCommerce
Experience5 Years
DegreeMaster
Offered Salary$56,160
LocationHybrid

Who's the hiring manager?

Sign up to PitchMeAI to discover the hiring manager's details for this job. We will also write them an intro email for you.

Uncover Hiring Manager

Job Description

About BeOne Medicines

BeOne Medicines continues to grow at a rapid pace, offering challenging and exciting opportunities for experienced professionals. We seek scientific and business professionals who are highly motivated, collaborative, and, most importantly, share our passionate interest in fighting cancer.

Internship Program Dates

June 8 - August 21, 2026

Education Required

Currently obtaining an undergraduate degree in the life sciences or other related field.

General Description

BeOne Medicines is a global biopharmaceutical company dedicated to the discovery and development of innovative drug therapies for the treatment of cancer. The Regulatory Affairs group is seeking a Regulatory Affairs Summer Intern to work closely with the North America Regulatory Affairs team.

Specifically, the intern will:

  • Work on programs and strategies for compounds in multiple stages of development.
  • Gain experience and exposure in drug development intended to address unmet medical needs in markets globally through an understanding of laws, guidance, and regulatory requirements for drugs and combination products.
  • Use creative problem-solving skills to develop new ideas and insights, including takeaways about yourself as a leader.
  • Partner with other regulatory team members with diverse skills and experiences in building solutions for real-life business challenges through hands-on projects.

Essential Functions Of The Job

  • Collaborate with the US Regulatory Affairs team members in providing regulatory guidance to cross-functional teams.
  • Support and attend Regulatory Team meetings with the Regulatory lead.
  • Participate in cross-functional team meetings and support the drafting, review, and approval of regulatory deliverables.
  • Support colleagues in handling submissions as needed and tracking documents’ status.
  • Support the archiving of official submissions and correspondence with different Health Authorities in the BeiGene document management system.
  • Participate in project teams, as determined by the supervisor.

Supervisory Responsibilities

No

Computer Skills

Proficient in Microsoft Office

Other Qualifications

  • Ability to communicate and write English clearly, concisely, and effectively.
  • Well-organized, with an ability to prioritize tasks.
  • Independently motivated, with good problem-solving ability.
  • Excellent interpersonal skills; a team player.

Travel

None

Pay Rates

Bachelors: $27/hour USD

Global Competencies

BeOne Medicines values Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit. Through our twelve global competencies, we aim to deliver more affordable medicines to patients worldwide:

  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Key skills/competency

  • Regulatory Affairs
  • Drug Development
  • Clinical Trials
  • FDA Regulations
  • Document Management
  • Cross-functional Collaboration
  • Problem-Solving
  • Communication Skills
  • Life Sciences
  • Project Support

Tags:

Regulatory Affairs Intern
regulatory guidance
drug development
submissions
cross-functional collaboration
document management
problem-solving
compliance
health authorities
program strategies
scientific communication
Microsoft Office
Word
Excel
PowerPoint
document management systems

Share Job:

How to Get Hired at BeOne Medicines

  • Research BeOne Medicines's culture: Study their mission, values, recent news, and employee testimonials on LinkedIn and Glassdoor.
  • Customize your resume: Tailor your resume to highlight relevant coursework, research, and any experience demonstrating attention to detail and collaboration, specifically for Regulatory Affairs Summer Intern roles.
  • Showcase your passion: Emphasize your genuine interest in fighting cancer and contributing to innovative drug therapies during your application and interviews at BeOne Medicines.
  • Prepare for regulatory discussions: Familiarize yourself with basic drug development phases and the role of regulatory affairs in the pharmaceutical industry to impress during interviews.
  • Highlight key competencies: Be ready to provide examples demonstrating teamwork, problem-solving, initiative, and clear communication, aligning with BeOne Medicines's global competencies.

Frequently Asked Questions

Find answers to common questions about this job opportunity

Explore similar opportunities that match your background