Regulatory Affairs Specialist, Medical Device

abbott· 3808 ABT Med(Malaysia)Sdn Bhd
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📍 Vietnam - HanoiFull time

About this role

     

JOB DESCRIPTION:

ABOUT ABBOTT

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

WORKING AT ABBOTT

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:

  • Career development with an international company where you can grow the career you dream of.

  • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.

  • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

Main Purpose of Job:

Responsible for activities which lead to and maintain regulatory approval to market devices. Works with various stakeholders such as labeling / global team for launch readiness.

Develops and implements strategies for earliest possible approvals.

Ensures timely preparation of submissions. Builds rapport with regulatory agencies. Anticipates regulatory environment change and manages the regulatory intelligence for new policy, regulation etc. as required.

Key Responsibilities:

  • Manage the regulatory approval or registration of medical devices and license maintenance.
  • Develop registration strategies, prioritizing assignments, implementing regulatory plan, and coordinating multiple projects and activities in accordance with strategic company objectives, submission plan and targets.
  • Research and monitors regulatory requirements for assigned geographies / competent authority
  • Monitor requirements of related medical device laws & regulations
  • Cultivation of professional working relationships with competent authorities and local medical device industry association
  • Review and approval of A&P materials to ensure compliance with local regulations.
  • Ensure proper documentation and record management of submission, approvals, certificates as required.
  • Handle/supports regulatory related processes or projects, e.g. labeling project, PRA process

Qualifications / Education Required:

  • Diploma, Advanced/Higher/Graduate Diploma, Bachelor’s degree or equivalent, preferrably in pharmacy, health sciences or related science background  

Skills and Experience:

  • 2 years experience in Medical Device Regulatory Affairs preferred.
  • Proficient in Microsoft Office applications especially excel files.
  • Effective interpersonal, communication and analytical skills
  • Proficiency in written and spoken English and Local language.
  •  Independent. Highly result oriented; ability to deliver and overcome obstacles.

     

The base pay for this position is

N/A

In specific locations, the pay range may vary from the range posted.

     

JOB FAMILY:

Regulatory Operations

     

DIVISION:

MD Medical Devices

        

LOCATION:

Vietnam > Hanoi : Handi Resco Tower

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

Standard

     

TRAVEL:

Not specified

     

MEDICAL SURVEILLANCE:

Not Applicable

     

SIGNIFICANT WORK ACTIVITIES:

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

     

     

     

Frequently Asked Questions

Is the salary disclosed for the Regulatory Affairs Specialist, Medical Device position at abbott?
The salary for this Regulatory Affairs Specialist, Medical Device role at abbott is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Regulatory Affairs Specialist, Medical Device position at abbott located?
This Regulatory Affairs Specialist, Medical Device role at abbott is based in Vietnam - Hanoi. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Regulatory Affairs Specialist, Medical Device role at abbott full-time or part-time?
This is listed as a Full time position. It is posted as a Regulatory Affairs Specialist, Medical Device role in the 3808 ABT Med(Malaysia)Sdn Bhd department at abbott.
Which team or department does the Regulatory Affairs Specialist, Medical Device at abbott belong to?
This Regulatory Affairs Specialist, Medical Device position is part of the 3808 ABT Med(Malaysia)Sdn Bhd department at abbott. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Regulatory Affairs Specialist, Medical Device position at abbott?
Click the "Apply Now" button on this page. You will be redirected to abbott's official application portal hosted on workday where you can submit your application directly.
When was the Regulatory Affairs Specialist, Medical Device job at abbott posted?
This Regulatory Affairs Specialist, Medical Device position at abbott was posted on Aug 25, 2026. Apply as soon as possible — early applications are often reviewed first.
Regulatory Affairs Specialist, Medical Device
abbott
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