# Quality & Regulatory Specialist

> SOFMEDICA · Uzbekistan, Uzbekistan (Hybrid) · Full-time · Posted 2026-05-29

**Workplace:** hybrid

**Department:** Compliance

## Description

SOFMEDICA is a leading regional multinational company that distributes innovative medical equipment harnessing the power of precision to improve healthcare outcomes. We are deeply committed to bridging the gap between cutting-edge medical technology and patients in Central and Southeastern Europe.

We are lexpanding our operations in Uzbekistan and we are looking for a Quality and Regulatory Specialist to join our team and contribute to the quality and compliance of our medical devices.

**Responsibilities:**

-   Manage and coordinate the registration, renewal, variation, and maintenance of product registrations in Uzbekistan.
-   Prepare, review, submit, and follow up on regulatory dossiers and required documentation with competent authorities.
-   Monitor changes in local regulatory requirements and assess their impact on company products and operations.
-   Maintain effective communication with regulatory authorities, certification bodies, and other relevant institutions.
-   Ensure that product certificates, technical documentation, declarations, approvals, and registrations are accurate, valid, and properly archived.
-   Support the business with regulatory advice related to product launches, imports, distribution, labeling, and documentation requirements.
-   Manage and maintain the company’s **Quality Management System** in accordance with standards. internal procedures, and applicable regulatory requirements.
-   Ensure quality processes are properly documented, implemented, monitored, and continuously improved.
-   Maintain quality records, procedures, work instructions, forms, certificates, and technical files to ensure compliance, traceability, and audit readiness..

## Requirements

-   University degree in Pharmacy, Life Sciences, Engineering, Quality Management, Regulatory Affairs, or a related field.
-   Previous experience in regulatory affairs, quality assurance, product registration, or compliance, preferably in medical devices, pharmaceuticals, healthcare, diagnostics, or another regulated industry.
-   Good understanding of Quality Management Systems
-   Knowledge of regulatory requirements in Uzbekistan would be a strong advantage.
-   Experience with documentation control, complaint handling, CAPA, audits, and supplier qualification.
-   Experience communicating with competent authorities or certification bodies is preferred.
-   High level of integrity, accountability, and confidentiality.
-   Proficiency in Microsoft Office and document management tools.
-   Fluency in Uzbek and/or Russian; good command of English is preferred.

## Benefits

We offer a competitive compensation and benefits package, professional development opportunities, and the chance to work in a dynamic international environment. The role provides strong exposure to regulatory affairs, quality management systems, audits, supplier quality, and product compliance, with opportunities for continued career growth within the organization.

## Apply

[Apply at SOFMEDICA](https://apply.workable.com/sofmedica/j/5972A13675/apply)

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