Qualified Person

An established organization is seeking a Qualified Person who will be responsible for the certification of batches, ensuring full compliance with GMP standards and internal quality procedures. The role plays a key part in overseeing quality systems and supporting continuous operational excellence.

Key Responsibilities

• Certify batches for release in accordance with GMP and company procedures.
• Oversee quality assurance processes and ensure compliance with all relevant regulatory requirements.
• Review and approve batch records, validation documentation, deviations, complaints, and change control activities.
• Provide final approval of new material suppliers.
• Identify the need for new or revised written procedures across all stages of the batch release process.
• Collaborate with cross-functional teams to resolve quality-related issues and ensure long-term prevention.
• Remain up to date with industry trends, regulatory developments, and quality management best practices.

Requirements

• University degree in Pharmacy, Chemistry, Chemical Engineering, or a related scientific field.
• Registered Qualified Person status according to EOF regulations is considered an asset.
• Minimum 5–6 years of experience in Quality Assurance or Quality Control.
• Strong knowledge of GMP, regulatory frameworks, and quality systems.
• Excellent communication and interpersonal skills for effective cross-functional collaboration.
• Strong managerial and decision-making skills.
• High attention to detail and commitment to high-quality standards.
• Fluency in Greek and English, written and spoken.
• Experience with regulatory inspections and maintaining compliance with relevant authorities.

What the Organization Offers

• Competitive compensation package
• Private health insurance
• Stable, well-structured, and supportive working environment
• Opportunities for ongoing learning and professional development
• Participation in a collaborative team committed to high-quality standards