Qualified Person (QP)

Position: Qualified Person (QP)

Location: Emilia-Romagna, Italy

Company: Confidential – European Pharmaceutical Logistics Provider

About the Company

While the organization remains confidential, it is recognized for its long-standing reputation in pharmaceutical logistics and regulatory compliance . With a people-first culture and strong growth across Europe, it provides a stable yet agile work environment where quality is a shared value.

Role Overview

A leading logistics provider operating across the European healthcare supply chain is currently looking for an experienced and proactive Qualified Person (QP) to strengthen its Quality Assurance team in Emilia-Romagna . This is an excellent opportunity to take on a key role in ensuring the integrity of pharmaceutical products and compliance with regulatory requirements in a fast-paced, growth-oriented environment.

As a Qualified Person , you will be entrusted with overseeing and safeguarding the quality and compliance of pharmaceutical goods across international operations. You will ensure that all processes adhere to strict industry regulations and support the organization’s continued commitment to excellence and safety.

Your Responsibilities

• Guarantee full compliance with applicable EU GMP/GDP standards and national regulations
• Supervise quality activities at a site authorized for physical importation under a valid MIA license
• Lead the implementation and oversight of QA practices including deviation and change control management, validation, and documentation control
• Monitor external suppliers and support customer qualification processes
• Drive continuous improvement by identifying risks and implementing preventive or corrective measures
• Act as a liaison with regulatory bodies and represent the site during inspections and audits
• Provide subject matter expertise to internal teams on all matters related to pharmaceutical quality assurance

Profile of the Ideal Candidate

• Legally recognized as a Qualified Person in Italy
• Minimum of 5 years of relevant experience in a QA role within pharmaceutical logistics, manufacturing, or distribution
• Solid understanding of Good Manufacturing Practice (GMP) , GDP, and quality systems management
• Previous exposure to MIA-licensed operations and international product importation processes is preferred
• Self-directed, detail-oriented, with a strong sense of responsibility and ethical commitment
• Fluent in Italian and English ; comfortable working in bilingual environments

What’s Offered

• Competitive remuneration package , complemented by a range of benefits
• A professional and collaborative workplace where your contribution directly supports public health
• Opportunities to engage in continuous learning , professional development, and internal mobility
• A position within a solid, internationally active organization driven by quality, innovation, and long-term vision

Interested?

If you're ready to take on a high-impact role in an evolving sector, please submit your CV along with a short cover note. All applications will be treated with the strictest confidentiality.