Intern- Regulatory Affairs

MSD

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profile Job Location:

Singapore - Singapore

profile Monthly Salary: Not Disclosed
Posted on: 09-11-2025
Vacancies: 1 Vacancy

Job Summary

Job Description

Support activities related to specific short term projects.

Contribute to the planning and execution of registration strategies for medicinal products in Singapore and Brunei to ensure timely and successful registration outcome.
Assist with variation submissions and follow through with Regulatory Agency (Singapore and Brunei) until approval.
Create artworks for variation submission and commercialization post Regulatory Agency approval in accordance with Singapore and Brunei regulations and internal procedures.
Certificate of pharmaceutical product processing.
Maintain and update internal regulatory affairs databases and systems.
Support regulatory team with other administrative tasks.
Manage document archival.
Review for product listings for Zuellig and PV
Support tender and renewal requirements and provide information/document support
Support invoicing processing and SOP reviews.
Involve in digital initiatives
Clean up of archival documents where necessary.

Required Skills:

Accountability Accountability Adverse Event Report Art Creation Audits Compliance Business Registrations Business Strategies Commercialization Data Quality Assurance Document Control Systems Drug Registration Electronic Common Technical Document (eCTD) Employee Training Programs Mentorship Patient Registration Policy Implementation Product Registrations Project Management Records Retention Management Regulatory Affairs Compliance Regulatory Affairs Management Regulatory Applications Regulatory Communications Regulatory Compliance Regulatory Compliance Audits 2 more

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.

Employee Status:

Intern/Co-op (Fixed Term)

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

01/30/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Required Experience:

Intern

Job DescriptionSupport activities related to specific short term projects. Contribute to the planning and execution of registration strategies for medicinal products in Singapore and Brunei to ensure timely and successful registration outcome. Assist with variation submissions and follow through wit...
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Key Skills

  • Proofreading
  • Adobe Acrobat
  • FDA Regulations
  • Manufacturing & Controls
  • Biotechnology
  • Clinical Trials
  • Research & Development
  • GLP
  • cGMP
  • Product Development
  • Chemistry
  • Writing Skills

About Company

Company Logo

Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more

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