# Quality Assurance Supervisor

> CURITY PHARMA · Larissa, Greece · Full-time · Posted 2026-11-11

**Workplace:** on_site

**Department:** Quality Assurance

## Description

The Quality Assurance Supervisor is responsible for supervising daily QA operations to ensure compliance with Good Manufacturing Practices (GMP), applicable regulatory requirements, and internal Quality Management System (QMS) standards. The role ensures product quality, regulatory compliance, and continuous improvement across manufacturing and quality operations.

**Key Responsibilities**

-   Supervise daily QA operations and coordinate QA team activities
-   Maintain oversight of Quality Management System (QMS) processes
-   Ensure compliance with EU GMP regulations, and internal procedures
-   Create, review and approve quality documentation, including SOPs, protocols, and reports
-   Oversee management of deviations, complaints, investigations, CAPAs, training activities and Change Controls
-   Ensure effective implementation and follow up of CAPA Activities
-   Review batch manufacturing records and ensure compliance with specifications
-   Support batch release activities in coordination with QA Management/Qualified Person
-   Participate in internal and external audits, as well as regulatory inspections
-   Ensure timely investigation and escalation of quality issues to QA Management
-   Provide training, guidance, and performance feedback to QA personnel
-   Collaborate closely with Production, QC, RnD, and other departments to ensure efficient operations within timeframes
-   Support continuous improvement initiatives within the QMS
-   Promote compliance culture, data integrity, and risk-based thinking
-   Ensure readiness of QA Systems for regulatory inspections
-   Supervise QA personnel and allocate daily tasks
-   Support operational teams in quality related issues and decisions

## Requirements

**Required Qualifications**

-   Bachelor’s degree in Pharmacy, Chemistry, Biology, Chemical Engineering or related scientific field
-   3–5+ years of experience in Quality Assurance within a GMP-regulated pharmaceutical environment
-   Strong knowledge of EU GMP, and regulatory requirements
-   Experience in QMS processes (deviations, CAPA, change control, complaints)
-   Fluency in English (written and spoken)
-   Previous experience in a supervisory or team lead role is considered as an asset

**Skills & Competencies**

-   Strong leadership and team management abilities
-   Excellent attention to detail and quality mindset
-   Strong analytical and problem-solving skills
-   Ability to manage multiple priorities under pressure
-   Effective communication and cross-functional collaboration
-   High level of integrity and compliance awareness
-   Risk-based thinking and decision-making capability

## Apply

[Apply at CURITY PHARMA](https://apply.workable.com/curity/j/647EF70827/apply)

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