Overview
Merck’s Regional Regulatory Operations – Asia Pacific (RRO-AP) is seeking an enthusiastic intern to support regulatory publishing and process innovation initiatives. This internship provides hands-on experience in regulatory dossier management, process optimization, and the application of digital tools to improve operational efficiency in the pharmaceutical industry.
What You'll Get Out of This Internship
- Practical exposure to regulatory dossier publishing and international submission standards
- Hands-on experience with Regulatory Information Management (RIM) systems
- Insight into process innovation, automation solutions, and data-driven decision-making
- Opportunities to collaborate with global, regional, and local teams
- Professional growth through participation in cross-functional projects and events
Key Responsibilities
Submission Publishing (30%)
- Assist Regional Publishers in preparing and submitting regulatory dossiers to health authorities
- Maintain submission templates and ensure compliance with regional and country requirements
System Process & Regulatory Innovation (SPRI) (60%)
- Organize regional Community of Practice (CoP) and Process & Digital Forum (PDF) sessions
- Develop small-scale automation solutions to improve operational efficiency
- Collect, analyze, and visualize data to support business process improvements
- Manage document templates, access controls, and security in content and labeling systems
- Provide logistical support for the 2026 SPRI Synergy event, enhancing cross-functional collaboration
Other Responsibilities (10%)
- Assist with organizing internal meetings, maintaining SharePoint, and suggesting process improvements
Requirements
- Current student pursuing a degree in a related field
- Proficient in Microsoft Office, particularly Excel
- Strong analytical skills, with the ability to collect, process, and present data
- Detail-oriented, organized, and able to manage multiple tasks simultaneously
- Effective communication and collaboration skills for cross-functional teamwork
Preferred Skills
- Understanding of regulatory compliance, eCTD submissions, document control, and data quality assurance
- Familiarity with process optimization and automation solutions
Who This Internship is Ideal For
- Students interested in regulatory operations, data analysis, and process innovation in the pharmaceutical industry
- Individuals who enjoy structured workflows and improving operational efficiency
- Candidates eager to gain hands-on experience with regulatory systems and cross-functional collaboration
About Company
Merck & Co., Inc., also known as Merck Sharp & Dohme LLC, is a global leader in healthcare, committed to innovation, quality, and operational excellence. The Regional Regulatory Operations – Asia Pacific team leverages advanced systems and data-driven approaches to ensure timely, compliant regulatory submissions and continuous process improvements.
Internship Details
- Location: Hybrid (Asia Pacific)
- Duration: Fixed-term internship; dates as per academic schedule
- Department: Regional Regulatory Operations – APAC
- Training Provided: Yes, with mentorship and exposure to global regulatory practices
- Flexible work arrangements; some travel may be required
