Abbott Posted August 22, 2026

Senior Regulatory Affairs Executive - Pharmaceuticals Division

Thuan An, Bình Dương, Vietnam FULL_TIME
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Abbott is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

ABOUT ABBOTT

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

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.

In Vietnam, Abbott’s Established Pharmaceuticals Division has committed to enhance the care of patients. Our products cover several therapeutic areas, including gastroenterology, women health, cardiology, primary care, specialty and food supplement. Our key prescription products include Lipanthyl, Klacid, Duphaston, Drosperin and BetaSerc. Our key over-the-counter products are Duphalac, CG210, Estraceptin, Brufen, Fatig, Surbex. We also have the Influvac vaccine.

MAIN PURPOSE OF ROLE

• Experienced professional individual contributor that works under limited supervision.

• Apply subject matter knowledge in the area of Regulatory Affairs.

• Require capacity to apply skills/knowledge within the context of specific needs or requirements.

• Handle process of registration of new products, maintenance of all approved products in Vietnam and operate marketed products according to local regulations.

MAIN RESPONSIBILITIES

Registration of New and Existing Products

• Reviews and compiles registration dossier for prompt renewal/initial/ variation registration

• Ensures availability of updated registration documents/samples

• Fast requisition of dossier and check requests

• Initiates/monitors/updates Regulatory Report in timely manner

Registration of Promotion Materials

• Register and compiles registration dossier for promotional material

• Ensures all promotional materials are lawfully compliance

Regulatory Intelligence

• Be aware of coming new regulation/change that impact to regulatory or business

• Inform head of Department/contacts all change and upcoming new regulations

• Implement new regulation properly

Regulatory Compliance

• Ensures that all exempt regulated products are MOH verified prior to production use

• Ensures that all product labels/package inserts are updated as approved by MOH's regulation.

• Keeps registration record updated at all times and promptly submits books and records as per schedule

Cross-function Support

• Ensures prompt coordination with other departments/units such as Sales & Marketing on regulatory and corporate matters

• Ensures correctness of received documents vs information submitted

Administrative

• Ensures that all technical documents/dossiers and registration samples are kept in secured place

• Maintains proper filing of protocol and other regulatory and clinical related documents

• Keeps updated files of MOH Regulations

BACKGROUND/ EXPERIENCE REQUIRED

• Bachelor of Pharmacy

• Strong knowledge of Vietnamese pharmaceutical regulations.

• Minimum 5 years of experience in Regulatory Affairs, preferably with a local pharmaceutical company.

• Experience in R&D or QA or QC will be an added advantage.

• Language skills: Vietnamese, English

• Computer skills: MS Office

Job details

Seniority
Senior
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Thuan An, Bình Dương, Vietnam
Employment type
FULL_TIME

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 101 comparable Senior Regulatory Affairs roles across 42 biopharma companies.

101Comparable roles tracked
90Currently active
42Companies hiring similar roles
21Countries represented

Salary context

37 of 101 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Senior Regulatory Affairs Specialist · Johnson & Johnson $79,000/yr – $127,650/yr
Highest disclosed · Senior Principal Scientist, Regulatory Liaison · Merck $190,800/yr – $300,300/yr
Peer group range $103,325 – $245,550 (median $205,000)

Where these roles are based

Top locations among the 101 comparable roles

United States53
India6
China4
United Kingdom4
Poland4
Japan4

+ 15 more countries

Seniority mix

101 of 101 peers have a known seniority level

Senior45
Associate Director43
Principal13

Therapeutic area mix

12 of 101 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology6
Immunology2
Dermatology & Aesthetics2
Vaccines & Infectious Disease1
Rare Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

45%similar
Mylan, Lda. Lisbon, Portugal Senior
Same function Same seniority
45%similar
Mylan, Lda. Lisbon, Portugal Senior
Same function Same seniority
45%similar
Pfizer Inc. (Philippines) Makati City, Philippines Senior
Same function Same seniority
45%similar
BMS Services Sp. z o.o. Warsaw-WeWork-PL, Poland Senior
Same function Same seniority
45%similar
Amgen Asia Holding Limited China, Hong Kong Senior
Same function Same seniority
45%similar
Amgen Technology Pvt Ltd. Hyderabad, India Senior
Same function Same seniority

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

45%
Senior Specialist Regulatory Operations and System Support
Mylan, Lda. · Lisbon, Portugal · Senior
Function Therapeutic area Seniority Country
45%
Senior Specialist, Document Management
BMS Services Sp. z o.o. · Warsaw-WeWork-PL, Poland · Senior
Function Therapeutic area Seniority Country
45%
Sr Mgr Regulatory Affairs
Amgen Technology Pvt Ltd. · Hyderabad, India · Senior
Function Therapeutic area Seniority Country
45%
Sr. Regulatory Specialist
Roche · Beijing, Beijing, China's Mainland · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.