Intern- Regulatory Affairs- CMC

MSD; Singapore; Hybrid; SGD 17,000 - 23,000; Part time

Benefits offered by this job

Hybrid work model

Internship 6 months

Job summary

MSD in Singapore offers a 6-month, fixed-term internship in regulatory affairs, with hybrid work (virtual/on-site) and the January 2027 intake. You will execute APAC submissions, develop regulatory strategies, liaise globally, and review packages while contributing to policy and advocacy efforts.

You’ll gain hands-on regulatory Science experience in a diverse team. The role targets students in scientific disciplines, seeking growth through practical regulatory exposure and collaboration on

Qualifications

• Diploma or BSc in a scientific discipline (e.g., Chemistry, Biology, Engineering)
• Fluency in an additional APAC-region language is a plus

Responsibilities

• Generate regulatory strategies
• Liaise with colleagues globally
• Review submission packages
• Deliver on operational excellence projects
• Develop best practices for regulatory science
• Learn and apply regulatory policy and advocacy
• Provide ad-hoc support as needed

Skills

Regulatory affairs

Data analysis

Attention to detail

Documentation

Cross-functional collaboration

Regulatory submissions

eCTD knowledge

Education

Diploma or BSc in a scientific discipline

Tools

eCTD knowledge

Job description

Job Description

Our company starts your journey on the career path within the pharmaceutical industry. Not only will you learn skills both technical and professional but work on projects that will contribute towards enhancing people’s lives across the world.

You will be part of a diverse and inclusive, and multi-skilled team of highly motivated individuals. We keep patients at the very heart of all that we do and strive to find solutions and treatments for some of the world’s most challenging healthcare needs.

So, what will you be responsible for?

The Intern will be involved in and responsible for the execution and management of the APAC region submissions including new product registrations and life-cycle submissions to keep our products compliant and available for patients.

In this role you will be working to

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

Additionally, you will

• Work alongside our team to deliver on operational excellence projects
• Work alongside our team in developing best practises for regulatory science
• Learn and apply regulatory policy and advocacy
• Provide ad-hoc support as needed

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

You will be looking to complete a 6-month placement in your third or penultimate year of study, returning to your course at the end of the placement.

The ideal person will have

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

Qualities we look for…

• Communicates, participates and collaborates as one team; winning and losing together
• Focuses on what matters the most to create the greatest value for patients
• Acts with urgency, rigor and determination to enable us to continue to deliver our medicines and vaccines around the world
• Is intellectually curious, adapts and has a commitment to never give up, whether we succeed or fail
• Aligns with and fosters a culture of diversity and inclusion; being part of an inclusive environment where everyone is able to contribute their best ideas
• Encourages curiosity, voices their opinions and engages in healthy debate to improve ideas and decisions to achieve better outcomes
• This role is for the January 2027 intake

Required Skills

Analytical Problem Solving, Analytical Problem Solving, Analytical Thinking, Analytical Tools, Audits Compliance, Biology, Chemical Engineering, Compliance Investigations, Critical Thinking, Data Quality Assurance, Decision Making, Detail-Oriented, 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 {+ 6 more}

Employee Status

Intern/Co-op (Fixed Term)

Flexible Work Arrangements

Not Applicable

Job Posting End Date

11/30/2026

Requisition ID

R413709