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Septodont

Regulatory Affairs Associate

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  • Posted a month ago
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Job Description

About Septodont:

At Septodont, we are spreading smiles worldwide. With over 90 years plus of excellence globally & 25 years domestically, we&aposve been at the forefront of revolutionizing dental care worldwide. Our commitment to quality, innovation, and patient well-being drives us to continually push the boundaries of dental science. As a global leader in dental solutions, we&aposre dedicated to empowering dental professionals and improving patient outcomes everywhere.

Septodont communicates a culture of growth and opportunity, enticing top talent to join its dynamic team. With a focus on nurturing talent, fostering creativity, and promoting diversity in the workplace, Septodont presents itself as a people-oriented employer that looks after the professional development of its team. Aspiring candidates are drawn to the company&aposs reputation for fostering a collaborative environment where ideas flourish and individuals thrive.

Scope of role: Vietnam/Cambodia/Myanmar

JOB SUMMARY

The Regulatory Affairs Associate supports regulatory affairs activities by handling registration and maintenance of our portfolio, ensuring compliance with health authorities&apos requirements, and maintaining registration tracking systems. This role will have experience not only working in RA but also PV & QA.

KEY ACCOUNTABILITIES

Regulatory Affairs (70%):

  • Representative on behalf of Corporate Regulatory Affairs of Septodont; be interface between local authorities and Septodont.
  • Registration Documentation Management and Verification: Prepare, compile, and orchestrate comprehensive registration files with cross-functional teams, conducting quality checks to ensure compliance with local and international regulatory standards. Help in collecting prerequisites, and other requirements for RA submissions for Septodonts RA activities.
  • Registration Process Administration: Process registration applications, certificates, and correspondence, maintaining precise tracking of submission status and regulatory interactions. Collaborate and follow with RA consultants for Septodonts product registrations or life cycle maintenance activities.
  • Market Readiness Support: Guide operations and commercial teams through regulatory requirements until product launch, ensuring market compliance and readiness.
  • In collaboration with Septodont corporate RA and RA consultants for proposition of regulatory strategies of Septodont products and adjustments if necessary.
  • Collaborate with Septodonts distributors for local regulatory aspects such as inspection, requirements of compliance from local agencies, customs requests, serialization setup coordination, annual reports coordination, etc.
  • Create and/or check and help in validating the labels, artworks, and leaflets as well as local labels in compliance with the corporate proposition as well as local regulations.
  • Meeting with local authorities on behalf of Septodont.
  • Registration Archive and Information Management: Create and maintain structured filing systems for registration documentation, supporting efficient information retrieval and regulatory compliance.
  • Registration Status and Lifecycle Monitoring: Develop and maintain detailed tracking systems for product registrations, managing renewal timelines and ensuring continuous market access for product portfolios.
  • To set up a Regulatory intelligence watch system for assigned countries: monitoring local regulations and evaluation of impact for our existing or future products; ensure good understanding and interpretation of local regulation for Septodonts business; participate to local lobbying if necessary.

PV and QA (30%):

  • Local contact person with the GVD department for vigilance.
  • Maintenance of local QMS regarding vigilance.
  • Maintain the Quality Management System.
  • Ensure the right storage and transportation conditions.

Education :

  • Post Graduate or Bachelor&aposs Degree in Sciences (chemistry, pharmacy or health-related majors)

Experiences :

  • Minimum 5 years of similar experiences
  • Understanding the local Vietnam regulations on Drugs & Devices
  • Ability to travel within the assigned region

More Info

Industry:Other

Function:Regulatory Affairs

Job Type:Permanent Job

Date Posted: 20/08/2025

Job ID: 124265097

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Last Updated: 24-09-2025 04:04:27 AM
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