INTERNSHIP DETAILS

Assoc. Spclst., Regulatory Affairs

CompanyMSD
LocationSingapore
Work ModeOn Site
PostedJuly 21, 2026
Internship Information
Core Responsibilities
Support the planning and execution of registration strategies for medicinal products in Singapore and Brunei. Assist with variation submissions, artwork creation, and the maintenance of internal regulatory databases.
Internship Type
full time
Company Size
39575
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
About the Role

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:

Adverse Event Report, Art Creation, Audits Compliance, Commercial Regulatory, Data Quality Assurance, Document Control Systems, Electronic Common Technical Document (eCTD), Employee Training Programs, Pharmaceutical Manufacturing, Pharmaceutical Processing, Policy Implementation, Project Management, Records Retention Management, Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory Applications, Regulatory Communications, Regulatory Compliance, Regulatory Compliance Audits, Regulatory Management, Regulatory Strategy Development

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:

07/23/2026

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

Key Skills
Adverse Event ReportArt CreationAudits ComplianceCommercial RegulatoryData Quality AssuranceDocument Control SystemsElectronic Common Technical DocumentPharmaceutical ManufacturingPharmaceutical ProcessingPolicy ImplementationProject ManagementRecords Retention ManagementRegulatory Affairs ComplianceRegulatory ApplicationsRegulatory CommunicationsRegulatory Strategy Development
Categories
HealthcareScience & ResearchAdministrativeLegalManufacturing