# Officer Regulatory Affairs, Lifecycle Management

> Lavipharm · Paiania, Greece (Hybrid) · Full-time · Posted 2026-03-13

**Workplace:** hybrid

**Department:** Regulatory Affairs

## Description

Lavipharm is seeking an **Officer Regulatory Affairs for Lifecycle Management** based in Athens who will be responsible for ensuring marketed products maintain full legislative compliance. The accountabilities include preparing dossiers, managing timelines and supporting multi-market submissions.

### Key Responsibilities

-   Execute routine regulatory activities: renewals, variations, CTD/Module 1 preparation
-   Monitor and manage timelines for MA variations, post-authorization activities and renewal applications
-   Prepare and submit import/export applications for medicinal products
-   Review and update packaging materials and artworks in line with current guidelines
-   Maintain regulatory databases and departmental filing systems

## Requirements

-   BSc in Pharmacy, Chemistry, Biology or a related field
-   1–2 years of experience in a Regulatory Affairs role within the pharmaceutical industry
-   Familiarity with EU regulatory legislation and eCTD submission processes
-   Excellent command of the Greek and English language (written and spoken)
-   Very good computer literacy

## Apply

[Apply at Lavipharm](https://apply.workable.com/lavipharm/j/1111A38BEF/apply)

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