Careers at SAFIRA PHARMA FZ-LLC

Build Central Asia'spharmaceutical future

Join the team that takes modern medicines from a manufacturer’s portfolio to patients in five countries. International standards, real responsibility and room to grow.

Working here

Expert work with a visible result

SAFIRA PHARMA FZ-LLC works to the standards of the international manufacturers we represent. Our regulatory, market-access and commercial teams operate across five countries, and every specialist works alongside colleagues who know their field in depth — from dossier requirements to national tender rules.

The result of the work is tangible. A dossier you prepare becomes a marketing authorisation; a tender you win puts a modern medicine on a hospital shelf. People join us for the professional depth — and stay because they see their own effect on patient access across the region.

GrowthStructured development: training with partner manufacturers, regional projects and a clear path to senior roles.

TeamworkSmall expert teams across five countries that share knowledge instead of guarding it.

ImpactYour work decides which modern medicines reach patients in the region — and how soon.

Open positions

Where we are hiring now

Three roles are currently open across the region. If none matches your profile, send a general application below — we read every CV.

Responsibilities

Prepare and submit registration dossiers to the national authority of Turkmenistan, in coordination with our regional regulatory teams.
Manage the lifecycle of marketing authorisations: renewals, variations and re-registration.
Work with manufacturers’ regulatory departments on dossier gaps and responses to authority queries.
Track changes in national and EAEU regulatory requirements and brief the wider team.

Requirements

Degree in pharmacy, chemistry or life sciences.
Two or more years in regulatory affairs or registration of medicines or medical devices.
Working English and Russian; knowledge of the CTD dossier structure is an advantage.

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Responsibilities

Identify and approach international manufacturers whose portfolios fit Central Asian markets.
Build market-entry cases: registration pathway, pricing, competitive landscape and sales forecast.
Negotiate distribution and representation agreements together with the legal team.
Represent SAFIRA PHARMA FZ-LLC at industry exhibitions and partner meetings.

Requirements

Three or more years in pharmaceutical business development, licensing or distribution.
Confident financial modelling and negotiation skills.
Fluent English; Russian and Uzbek are an advantage.

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Responsibilities

Own the medical-equipment portfolio in Kazakhstan: positioning, pricing and launch plans.
Prepare technical specifications and documentation for government tender submissions.
Train clinical users and distributor sales teams on diagnostic equipment.
Collect market feedback and coordinate service and warranty questions with manufacturers.

Requirements

Three or more years in product management for medical devices or equipment.
Understanding of public procurement in Kazakhstan.
Fluent Russian and English; readiness for regional travel.

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Application

Send your application

Choose a role or apply on a general basis — attach your CV and tell us briefly where you see yourself. We respond to every application within five business days.

Prefer e-mail? Send your CV tooffice@safirapharma.com