# Quality Validation / Qualification Specialist

> Lavipharm · Paiania, Greece (Hybrid) · Full-time · Posted 2026-02-19

**Workplace:** hybrid

**Department:** Quality

## Description

Lavipharm is seeking a Quality Validation / Qualification Specialist, based in Athens, who will be responsible for compliance to GMP and regulatory requirements of facilities, utilities, equipment and computerized systems.

### Responsibilities

-   Plan, overview execution, review results and approve qualification and validation activities (DQ, IQ, OQ, PQ)
-   Ensure appropriate prioritization of validation activities regarding manufacturing equipment, utilities, facilities and computerized systems
-   Issue, review and approve validation protocols, reports and supporting documentation
-   Maintain validation status throughout the lifecycle of systems and equipment
-   Provide QA oversight for change control, deviations and CAPAs related to validation
-   Ensure application of risk-based approaches to validation/qualification activities

## Requirements

-   Bachelor’s degree preferably in Engineering or Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology or other relevant field
-   Postgraduate qualification (master’s degree or equivalent) in a relevant field is preferred
-   At least 5 years experience in Quality manufacturing/systems preferably in Human Pharma Industry
-   Excellent knowledge of the English language
-   Computer Literacy (MS Office etc)

## Apply

[Apply at Lavipharm](https://apply.workable.com/lavipharm/j/5A1500DA56/apply)

---
Powered by [Workable](https://www.workable.com)