INTERNSHIP DETAILS

Regulatory & Supply Chain - Internship

CompanyBiomed Global
LocationPetaling Jaya
Work ModeOn Site
PostedOctober 1, 2026
Internship Information
Core Responsibilities
The intern will assist with MSDS compilation, regulatory status assessments, and supply chain housekeeping. They will also support the team with database maintenance, labeling implementation, and general regulatory process improvements.
Internship Type
internship
Company Size
304
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
For nearly three decades, Biomed Global has been a trusted leader in biomedical and life sciences across Malaysia and Singapore, with a vision of expanding throughout Asia. We specialize in delivering innovative medical solutions that enhance healthcare standards, support medical breakthroughs, and improve lives. With a team of over 300 experts, we partner with world-renowned brands to provide cutting-edge technologies to doctors, scientists, and hospitals. Recognized for our expertise, speed, and market knowledge, we aim to set the gold standard in the industry, driving advancements that shape the future of healthcare. At Biomed Global, we believe in transforming healthcare—one solution, one life, one breakthrough at a time. Biomed Global (M) Sdn. Bhd. 201601034878
About the Role
  • MSDS compilation for import clearance and poison item identification
  • MSDS translation into Bahasa Malaysia, in line with recent mandatory requirements by DOSH for all Health Institutions (Private & Government)
  • Poisons identification housekeeping (Scheduled Poisons under the Poisons Act)
  • Inter-departmental supply chain housekeeping support
  • Identify, check, and assess product regulatory status according to regulatory requirements (medical devices, poisons, hazardous substances & flammables)
  • Medical device certificates/licenses and Letters of Authorization files upkeep and re-organization
  • Assist in checking product local labeling implementation
  • Involvement in regulatory process improvements
  • Involvement in regulatory database management and maintenance
  • Assist the team with other ad-hoc regulatory matters



Requirements

  • Background from Medical Bio-science, Biomedical Science, Biotechnology.
  • Detail oriented.
  • Organized, good documentation practice.
  • Basic ability to use Microsoft Word, Excels, Power Point.
  • Good communication skills.
  • Agile and adaptable.
  • Good time management.

Key Skills
MSDS compilationRegulatory complianceSupply chain managementDocumentationMicrosoft WordMicrosoft ExcelMicrosoft PowerPointCommunication skillsTime managementData managementRegulatory assessmentLabeling implementation
Categories
HealthcareScience & ResearchLogisticsAdministrative