Senior Regulatory Affair Specialist

Hanoi Permanent
  • Join a leading medical devices company with well known portfolio in its category
  • Knowledgeable in medical regulatory affairs and quality management system

About Our Client

Our respectable client is a well known name in its category. Established in Europe and currently presents in more than 50 countries, they commit in medical technology development and expand their team aggressively, urgently look for Senior Regulatory Specialist for now.

Job Description

Report to RA Regional Manager (Expat) and dotted line manager in Vietnam, your responsibilities are as below but not limited to:

  • Hands-on local registration process with Regional exposure
  • Be the representative for the company to negotiate with MOH for approval, submitted application
  • Keep updated with government announcement, changes in regulatory policies & industry trends
  • Provide training to local team to ensure internal compliance
  • Keep an eye on medical product related activities, including: pre & post marketing events preview, field safety corrective actions, RA auditing

The Successful Applicant

  • Hold similar regulatory positions in medical devices
  • Bachelor's Degree in Biomedical Engineering/Chemistry/Pharmacy/Biology or related science degree.
  • Daily tasks involve English communication in both verbal and written
  • Actual experience and knowledge in Vietnam Medical Device Regulations
  • Positive working attitude with the team and also as individual

What's on Offer

Attractive compensation with great career development within the Group

Chau Ngo
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Job summary

What is your area of specialisation?
Healthcare / Pharmaceutical
Contract Type
Consultant name
Chau Ngo
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