Abbott Posted September 3, 2026

Regulatory affairs assistant

Tashkent, Toshkent, Uzbekistan FULL_TIME
Notify me about similar jobs

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, 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.

•    We are committed to bringing the benefits of our trusted medicines to more people in the world’s fastest-growing countries. Our broad portfolio of high-quality and differentiated branded generic medicines reaches across multiple therapeutic areas including gastroenterology, women's health, cardiometabolic, pain management/central nervous system, and respiratory.

•    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.

The Opportunity 

This position works out of our Tashkent location in the Established Pharmaceuticals Division.

What You’ll Do:

Arranging /ordering the   agreements   with   vendors/ Health Authorities, Power of Attorney , other   administrative documenta tion .

Arranging   translations,   notarizations using approved   vendor .

Proof-reading of documentation   in   local language and   English   – agreements with   vendors/ Health Authorities , Power of Attorney, artworks,   Methods of Quality Control,   approved registration documents,   regulatory documentation translations .

Visits to Health Authorities   – support in   submitting   documentation .

Support in printing, copying,   scanning of   documentation ,   preparation   of   documentation   for   mailing .

Support in preparation of documentation/dossiers/files for submission to Health Authorities.

Support   in filling and   maintaining   various   RA   tracking tables .

Work   in   corporate   electronic   systems .

Support during internal and external audits .

Requirements:

Higher education (p harmacy/chemistry /biology/biotechnology degree) .

English - intermediate ( verbal   &   written), Russian - intermediate, Uzbek - fluent.

Soft skills: ac curacy to details,   multi-tasking,   diligent, result-oriented,   ability to perform tasks in short timelines , proactive ,   responsible , ability to   learn   fast .

Hard skills : advanced   user   MS   Excel,   MS   Word, Adobe   Acrobat , Power   Point ; ability to learn   corporate   technical   system s.

Job details

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Tashkent, Toshkent, Uzbekistan
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 524 comparable Regulatory Affairs roles across 111 biopharma companies.

524Comparable roles tracked
497Currently active
111Companies hiring similar roles
46Countries represented

Salary context

128 of 524 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Consultant, Regulatory Science and Strategy · IQVIA $58,700/yr – $146,800/yr
Highest disclosed · Executive Director, Medical Writing · Regeneron Pharmaceuticals, Inc (USA) $285,600/yr – $475,900/yr
Peer group range $102,750 – $380,750 (median $201,450)

Where these roles are based

Top locations among the 524 comparable roles

United States211
India41
United Kingdom40
Japan35
Poland20
Ireland19

+ 40 more countries

Seniority mix

419 of 524 peers have a known seniority level

Manager164
Director73
Senior57
Associate Director52
Senior Director26
Intern/Fellow/Postdoc18
Associate12
Principal11
Executive/VP6

Therapeutic area mix

50 of 524 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Immunology17
Oncology12
Rare Disease7
Ophthalmology4
Vaccines & Infectious Disease4
Neuroscience3
Cardiovascular / CVRM2
Dermatology & Aesthetics1

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.

25%similar
Lilly Shanghai, Shanghai, China Associate Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
AbbVie Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

Open in 2 locations

North Chicago, United StatesFlorham Park, United States
25%similar
Novartis 本社, Japan
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Gilead Sciences K.K. Tokyo, Japan Manager
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Mylan Inc. Washington, United States Manager
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Generics [U.K.] Ltd. Lisbon, Portugal
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

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.

Or follow a whole field: get every new Regulatory Affairs job in Uzbekistan, and choose locations and companies.

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.

25%
Regulatory Affairs Associate Director
Lilly · Shanghai, Shanghai, China · Associate Director
Function Therapeutic area Seniority Country
25%
Development Regulatory Affaires (開発薬事) - Neuroscience, Gene Therapy & Precision Diagnostics
Novartis · 本社, Japan · Seniority not listed
Function Therapeutic area Seniority Country
25%
Artwork Coordinator
Generics [U.K.] Ltd. · Lisbon, Portugal · Seniority not listed
Function Therapeutic area Seniority Country
25%
Senior Manager, Regulatory Affairs CMC
McDermott Laboratories Limited · Northern Cross, Ireland · 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.