Intern- Regulatory Affairs- CMC

About the Role

Our company helps you build your career within the pharmaceutical industry. You’ll develop both technical and professional skills while working on projects that contribute to enhancing people’s lives around the world.

You will join a diverse, inclusive, and multi-skilled team of highly motivated individuals. Patients remain at the heart of everything we do as we work to find solutions and treatments for some of the world’s most challenging healthcare needs.

Internship Responsibilities

The Intern will be involved in the execution and management of APAC region submissions, including new product registrations and lifecycle submissions, to help keep products compliant and available for patients.

You will be working on the following:

• Generate regulatory strategies
• Liaise with colleagues globally
• Review submission packages

You will also:

• Work alongside the team to deliver operational excellence projects
• Support the development of best practices for regulatory science
• Learn and apply regulatory policy and advocacy
• Provide ad-hoc support as needed

Work Model

This internship will be completed in a hybrid model (virtual and/or on-site).

Placement Details

• 6-month placement in your third or penultimate year of study
• Return to your course at the end of the placement
• Role for the January 2027 intake

Required Qualifications

• Minimum of Diploma or BSc in a scientific discipline such as chemistry, biological sciences, engineering, or a related field (including, but not limited to: Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry) or an equivalent qualification
• Demonstrated analytical skills and a detail-oriented approach
• Fluency in an additional language commonly used in the APAC region is a plus

Qualities We Look For

• Communicates, participates, and collaborates as one team (“winning and losing together”)
• Focuses on what matters most to create the greatest value for patients
• Acts with urgency, rigor, and determination to deliver medicines and vaccines worldwide
• Is intellectually curious, adapts, and maintains a commitment to never give up
• Aligns with and fosters a culture of diversity and inclusion, enabling everyone to contribute their best ideas
• Encourages curiosity, voices opinions, and engages in healthy debate to improve ideas and decisions

Skills

Required Skills

• Analytical problem solving
• Analytical thinking
• Analytical tools
• Compliance investigations
• Critical thinking
• Data quality assurance
• Decision making
• Detail-oriented approach
• Documentation standards
• Document control systems
• Electronic Common Technical Document (eCTD)
• Liaison work
• Multidisciplinary teamwork
• Policy implementation
• Proactive thinking
• Records retention management
• Regulatory affairs management
• Regulatory CMC
• Regulatory communications
• Regulatory documents
• Regulatory management

Preferred Skills

Not specified.

Additional Information

• Employee Status: Intern/Co-op (Fixed Term)
• Flexible Work Arrangements: Not Applicable
• Job Posting End Date: 11/30/2026