# QC Supervisor Finished Products

> Lavipharm · Paiania, Greece · Full-time · Posted 2026-10-27

**Workplace:** on_site

**Department:** QC

## Description

Lavipharm is seeking a Supervisor of FP, based in Athens, who will be responsible for supervising the day-to-day testing and release-support activities of the FP QC team, ensuring analyses are performed accurately, on time, and in full compliance with cGMP, Good Documentation Practices (GDP) and data integrity requirements.

**Requirements**

-   Supervises and coordinates the daily activities of the Semi-Finished, FP Release and Stability Programs, Process, Analytical and Cleaning Validation analysis ensuring workload is prioritized to meet business objectives and defined timelines
-   Trains, develops and performs performance reviews of QC FP team members, ensuring they are equipped with the skills and knowledge to perform their roles effectively
-   Collaborates with QA, production, supply chain, RA, RnD and engineering teams to resolve quality-related issues and enhance product quality
-   Leads team Problem solving and troubleshooting sessions towards continuous improvement of QC Operations in FP
-   Monitors compliance of the FP team to all procedures, specifications, GMP and safety rules of the QC Laboratory
-   Champions Good Documentation Practices (GDP) and data integrity (ALCOA+) principles across the FP QC team, ensuring records are accurate, legible, contemporaneous, original and attributable
-   Leads as required and approves the investigation of OOS/OOT results
-   Reviews & Approves CoAs
-   Hosts and supports internal and external audits and regulatory inspections related to FP QC, ensuring timely and accurate responses
-   Owns and progresses deviations and change controls related to FP testing through to closure
-   Ensures instruments and computerized systems used for FP testing are properly qualified, maintained, calibrated and in proper operation, in accordance with applicable procedures

## Requirements

-   BSc in  Chemistry, Postgraduate degree in Pharmaceutical Science or related field is a plus

-   At least 10 years' experience in the Pharma industry within Quality Control operations, including exposure to FP testing
-   At Least 3 years in supervisory roles in QC Operations
-   Advanced Knowledge of the English language
-   Computer Literacy (MS Office, ERP System)
-   eQMS/eDMS experience will be considered a plus

## Apply

[Apply at Lavipharm](https://apply.workable.com/lavipharm/j/01EB8CA9A6/apply)

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