Our international pharmaceutical logistics partner is seeking an experienced Quality Assurance professional to take on the role of Site QA Specialist Qualified Person / Responsible Person within its GMP/GDP-regulated secondary packaging and distribution operations. In this strategic quality position, you will oversee the full quality system of a pharmaceutical distribution center, ensure regulatory compliance, and act as the primary QA contact for clients, authorities, and internal stakeholders.
Key Responsibilities:
- Fulfill all responsibilities and obligations assigned to the Qualified Person / Responsible Person under applicable national regulations
- Ensure adherence to GMP requirements during pharmaceutical repackaging operations and manage documentation required for the release or rejection of repackaged products
- Provide quality oversight of the secondary packaging site and all wholesale distribution activities performed at the facility
- Operate, maintain, and continuously improve the site quality management system
- Serve as the main point of contact for clients on all QA-related matters, including deviations, complaints, change control, and CAPA management
- Conduct GxP training sessions, ensure training compliance, and supervise QA-related learning activities
Key Requirements:
- University degree in Pharmacy (required)
- Relevant experience meeting the qualification criteria for QP/RP nomination
- Proven track record in a similar QP/RP role within a warehouse or logistics environment
- Strong experience with authority inspections, audits, and related preparation activities
- Proficiency in Hungarian and English
- Agile, proactive personality with strong communication and client-facing skills
If you are interested in this opportunity, please apply by submitting your CV
Our international pharmaceutical logistics partner is seeking an experienced Quality Assurance professional to take on the role of Site QA Specialist Qualified Person / Responsible Person within its GMP/GDP-regulated secondary packaging and distribution operations. In this strategic quality position, you will oversee the full quality system of a pharmaceutical distribution center, ensure regulatory compliance, and act as the primary QA contact for clients, authorities, and internal stakeholders.
Key Responsibilities:
- Fulfill all responsibilities and obligations assigned to the Qualified Person / Responsible Person under applicable national regulations
- Ensure adherence to GMP requirements during pharmaceutical repackaging operations and manage documentation required for the release or rejection of repackaged products
- Provide quality oversight of the secondary packaging site and all wholesale distribution activities performed at the facility
- Operate, maintain, and continuously improve the site quality management system
- Serve as the main point of contact for clients on all QA-related matters, including deviations, complaints, change control, and CAPA management
- Conduct GxP training sessions, ensure training compliance, and supervise QA-related learning activities
Key Requirements:
- University degree in Pharmacy (required)
- Relevant experience meeting the qualification criteria for QP/RP nomination
- Proven track record in a similar QP/RP role within a warehouse or logistics environment
- Strong experience with authority inspections, audits, and related preparation activities
- Proficiency in Hungarian and English
- Agile, proactive personality with strong communication and client-facing skills
If you are interested in this opportunity, please apply by submitting your CV