Responsibilities
-
Oversee quality assurance for the secondary packaging facility and wholesale distribution activities at the site
-
Ensure compliance with GMP requirements during pharmaceutical repackaging, including verification and provision of manufacturing documentation needed for product release or rejection
-
Operate and continuously improve the quality management system
-
Act as the primary point of contact for clients on quality-related matters (handling deviations, complaints, changes, CAPAs)
-
Provide GxP training and supervision of staff
-
Conduct risk assessments; manage the quality documentation system; oversee and approve SOP preparation
-
Manage suppliers and handle quality agreements, including their approval
-
Fulfill responsibilities as Qualified Person and Responsible Person in accordance with applicable national regulations
-
Serve as the key owner and operator of the site’s quality system in compliance with company policies as well as GMP/GDP guidelines
-
Provide professional leadership and guidance to colleagues working in quality assurance
-
Maintain effective communication with clients’ technical personnel and internal departments
Requirements
-
University degree, preferably in pharmacy
-
Experience required for QP/RP designation
-
Proven track record in a similar QP/RP role, preferably in a warehouse or logistics environment
-
Experience in regulatory inspections, audits, and preparation activities
-
Fluency in Hungarian and English
-
Advantage: prior leadership experience
-
Agile, change-oriented personality with strong client-facing and negotiation skills
Should you be interested in the opportunity please do not hesitate to submit your professional CV so we can contact you with the further details.
Responsibilities
-
Oversee quality assurance for the secondary packaging facility and wholesale distribution activities at the site
-
Ensure compliance with GMP requirements during pharmaceutical repackaging, including verification and provision of manufacturing documentation needed for product release or rejection
-
Operate and continuously improve the quality management system
-
Act as the primary point of contact for clients on quality-related matters (handling deviations, complaints, changes, CAPAs)
-
Provide GxP training and supervision of staff
-
Conduct risk assessments; manage the quality documentation system; oversee and approve SOP preparation
-
Manage suppliers and handle quality agreements, including their approval
-
Fulfill responsibilities as Qualified Person and Responsible Person in accordance with applicable national regulations
-
Serve as the key owner and operator of the site’s quality system in compliance with company policies as well as GMP/GDP guidelines
-
Provide professional leadership and guidance to colleagues working in quality assurance
-
Maintain effective communication with clients’ technical personnel and internal departments
Requirements
-
University degree, preferably in pharmacy
-
Experience required for QP/RP designation
-
Proven track record in a similar QP/RP role, preferably in a warehouse or logistics environment
-
Experience in regulatory inspections, audits, and preparation activities
-
Fluency in Hungarian and English
-
Advantage: prior leadership experience
-
Agile, change-oriented personality with strong client-facing and negotiation skills
Should you be interested in the opportunity please do not hesitate to submit your professional CV so we can contact you with the further details.

