CMC Regulatory Affairs Intern: Submissions & Strategy

MSD Malaysia

Greater London

Hybrid

GBP 17,000 - 23,000

Full time

3 days ago
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Benefits offered by this job

Hybrid work model

Job summary

MSD is offering a 12-month Regulatory Affairs CMC student placement in Moorgate, London, delivering hands‑on exposure to regulatory strategy, submissions management, health authority engagement, and operational excellence projects across the EMEA region.

You will support the execution of regulatory submissions, develop and review submission packages, collaborate with global and regional teams, and learn how to apply regulatory policies to ensure timely, compliant product life-cycle activities.

Qualifications

  • Currently studying at a UK university for a 12-month internship.
  • Working towards a BSc in a scientific or engineering discipline.
  • Strong communication and teamwork skills.
  • Demonstrates integrity, accountability and initiative.
  • Values diversity and inclusion in the workplace.

Responsibilities

  • Support the execution and management of regulatory submissions across the EMEA region.
  • Contribute to the development of regulatory strategies and submission packages.
  • Collaborate with global and regional teams to support regulatory objectives.
  • Learn and apply regulatory policies to ensure compliance with health authorities.
  • Support operational excellence and continuous improvement initiatives.
  • Participate in health authority engagement activities and develop digital skills.

Skills

Analytical Problem Solving
Regulatory Management
Communication
Teamwork
Data Analytics

Education

BSc or equivalent

Job description

MSD is offering a 12-month Regulatory Affairs CMC student placement in Moorgate, London, delivering hands‑on exposure to regulatory strategy, submissions management, health authority engagement, and operational excellence projects across the EMEA region.

You will support the execution of regulatory submissions, develop and review submission packages, collaborate with global and regional teams, and learn how to apply regulatory policies to ensure timely, compliant product life-cycle activities.

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