PFIZER (VIETNAM) LIMITED COMPANY Posted July 18, 2026

Labeling Operations Manager (LOM) – International Associate (12 Months Contract)

Viet Nam, Vietnam Full time
Regulatory Affairs Manager

PFIZER (VIETNAM) LIMITED COMPANY 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

Use Your Power for Purpose

As an Associate in International Labeling Operations at Pfizer, you will play a crucial role directly contributing to the improvement of patients' lives. Your work will ensure that our products are accurately labeled, meeting regulatory requirements and providing essential information to healthcare professionals and patients. This role offers a unique opportunity to make a tangible impact on global health while working with a team of dedicated professionals.

What You Will Achieve

In this role, you will:

Support preparation of labeling documents to ensure regulatory compliance.

Coordinate with cross-functional teams to gather necessary labeling information.

Support the maintenance of accurate records of labeling changes and approvals.

Support the development and implementation of labeling strategies.

Facilitate timely submission of labeling documents to regulatory authorities.

Contribute to project tasks and milestones, organizing work to meet deadlines.

Learn and apply basic team effectiveness skills within the immediate work team.

Make decisions within limited options to resolve basic problems under supervision.

Work in a structured environment using established procedures and seek guidance from colleagues.

Have work regularly reviewed for technical judgment, completeness, and accuracy, relying on supervisor's judgment.

Here Is What You Need (Minimum Requirements)

A BA/BS degree with 2-3+ years of experience

Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)

Basic understanding of regulatory requirements for labeling

Strong organizational skills

Excellent written and verbal communication skills

Ability to work independently and as part of a team

Attention to detail and accuracy

Ability to manage multiple tasks simultaneously

Basic project management skills

Bonus Points If You Have (Preferred Requirements):

Experience in the pharmaceutical or biotechnology industry

Familiarity with labeling software and databases

Knowledge of global labeling regulations

Experience with electronic document management systems

Strong interpersonal skills

Strong analytical skills

Ability to interpret and apply regulatory guidelines

Effective problem-solving skills

Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

Work Location Assignment: Hybrid

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Important Notice for Applicants

At Pfizer, we value your privacy and security. Please note:

All job applications must be submitted only through our official channels:

Pfizer Careers Website: Careers | Pfizer

Verified LinkedIn page: https://www.linkedin.com/

Verified local job board - Pharma360: Công ty dược tuyển dụng dược sĩ đại học - Việc làm dược sĩ Pharma360

We never request payment, bank details, or confidential personal information during the recruitment process.

If you receive suspicious messages or job offers outside these channels, please report them immediately to [ProtectPfizer@pfizer.com]

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on  Pfizer Careers .


Regulatory Affairs

Job details

Seniority
Manager
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Viet Nam, 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 145 comparable Manager Regulatory Affairs roles across 41 biopharma companies.

145Comparable roles tracked
135Currently active
41Companies hiring similar roles
23Countries represented

Salary context

37 of 145 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 Manager, Core Labeling Strategy · Mylan Inc. $95,000/yr – $193,000/yr
Peer group range $144,000 – $206,900 (median $180,500)

Where these roles are based

Top locations among the 145 comparable roles

United States58
India15
Japan10
Poland10
Ireland9
China7

+ 17 more countries

Seniority mix

145 of 145 peers have a known seniority level

Manager111
Associate Director26
Associate8

Therapeutic area mix

22 of 145 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology7
Dermatology & Aesthetics6
Neuroscience5
Immunology4

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.

60%similar
Novartis Vietnam, Vietnam Manager
Same function Same seniority Same country
45%similar
Lilly Shanghai, Shanghai, China Manager
Same function Same seniority
45%similar
Lilly Shanghai, Shanghai, China Manager
Same function Same seniority
45%similar
AbbVie Maidenhead, ENGLAND Manager
Same function Same seniority
45%similar
AbbVie Manager
Same function Same seniority

Open in 2 locations

Maidenhead, United KingdomMontreal, Canada
45%similar
AbbVie Singapore, sg Manager
Same function Same seniority

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.

60%
Regulatory Affairs Manager
Novartis · Vietnam, Vietnam · Manager
Function Therapeutic area Seniority Country
45%
Senior Regulatory Affairs Manager, Europe
AbbVie · Maidenhead, ENGLAND · Manager
Function Therapeutic area Seniority Country
45%
(Sr)Regulatory Affairs Manager
AbbVie · Taipei, tw · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager, Regulatory Affairs US & Canada Strategy Lead – Therapeutic Neurotoxins - Hybrid
AbbVie · Irvine, CA · Manager
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.