INTERNSHIP DETAILS

Assoc. Spclst., Regulatory Affairs

CompanyMSD
LocationChina
Work ModeOn Site
PostedJuly 29, 2026
Internship Information
Core Responsibilities
The intern will support the Regulatory Affairs team with product registration, life-cycle management, and cross-functional support for tender and quality processes. Additionally, the role involves handling pharmacovigilance tasks, medical affairs inquiries, and participating in industry seminars.
Internship Type
full time
Company Size
39572
Visa Sponsorship
No
Language
English
Working Hours
40 hours
Apply Now →

You'll be redirected to
the company's application page

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

The Pharmacy Internship Training Programme will be conducted under the supervision of the Regulatory Affairs Team for graduates of local accredited Bachelor of Pharmacy ("BPharm") Programs offered by The University of Hong Kong ("HKU") and The Chinese University of Hong Kong ("CUHK").


The Pharmacy Internship Training Programme covers various aspects across different departments, including:

·       Regulatory Affairs – To handle New Product Registration and product Registration Life-Cycle Management, with strategic planning for new launch and/or implementation of post-approval variation; Provide support to cross-functional teams such as Tender and In-Market Quality support.

·       Medical Affairs – To handle inquiry & patient program, experience to visit with HCP & symposium.

·       Pharmacovigilance – To handle AE reporting & if there is a need, to verify the data.

·       Others – Attending Drug Office seminar and/or Medical Device seminar, opportunities to work with different stakeholders, e.g. DOH officers, CPO, Legal Advisor etc.

Required Skills:

Adverse Event Report, Audits Compliance, Collaborative Development, Data Quality Assurance, Document Control Systems, Electronic Common Technical Document (eCTD), Employee Training Programs, Pharmacovigilance, Policy Implementation, Product Registrations, Records Retention Management, Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory Applications, Regulatory Communications, Regulatory Compliance, Regulatory Compliance Audits, Regulatory Strategy Development, Stakeholder Engagement, Strategic Management, Strategic Planning

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:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

10/30/2026

*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
Regulatory AffairsPharmacovigilanceAdverse Event ReportingRegulatory ComplianceStrategic PlanningProduct RegistrationStakeholder EngagementData Quality AssuranceAudits ComplianceDocument Control SystemsRegulatory Strategy DevelopmentPolicy ImplementationRegulatory CommunicationsCollaborative DevelopmentRecords Retention ManagementRegulatory Applications
Categories
HealthcareScience & ResearchManagement & Leadership