# QC Supervisor Finished Products

**Company:** [Lavipharm](https://jobs.workable.com/companies/xo7VDa4Gk15b3N2PMpZjbz.md)
**Location:** Paiania, Greece
**Workplace:** on site
**Employment type:** Full-time
**Department:** Quality

[Apply for this job](https://jobs.workable.com/view/36b1972a-9ca0-4f8b-b226-0da8717e0726)

## 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