Job summary

Job Responsibilities

• Handle regulatory activities for product registration (drugs, medical devices, veterinary drugs, biologicals, supplements) including new registration, variation, renewal, and withdrawal. Prepare and submit dossiers and liaise with Vietnamese authorities throughout the product lifecycle.
• Collaborate with Head Office for documentation and regulatory submission.
• Provide regulatory support and updates to internal teams and partners.
• Ensure legal compliance and support pharmacovigilance activities per SOPs and local regulations.
• Manage administrative tasks assigned by the Chief Representative.

Key Responsibilities:

• Act as the main contact with regulatory authorities and Head Office.
• Ensure timely and compliant submissions for registration and updates.
• Maintain regulatory records, licenses, and databases.
• Monitor and report adverse events and safety issues.
• Keep up-to-date with regulatory changes and industry trends.
• Support other departments and partners on regulatory matters.
• Attend meetings, trainings, and industry association events.
• Perform administrative tasks, manage office operations, and support visiting staff.

Experience requirements

• 3+ years of experience in regulatory affairs.
• Skills: Proficient in Microsoft Office, strong English and communication skills, project management.
• Attitude: Detail-oriented, team player, customer-focused, compliant.
• Willingness to travel for business or training as required.

Education requirements

• Degree in Pharmacy or related field.

Pls contact directly to our Consultant - Ms. Thu (Email: maithu.nguyen@adecco.com, Phone/Zalo: 0825955367) for more information.

Contact Person

• Thu Nguyen
• Adecco
• Tel.