As Qualified Person (QP), you will be responsible for securing that each batch of medicinal products has been manufactured and checked in compliance with the laws in force in that Member State and in accordance with the requirements of the marketing authorization. Furthermore, you certify in a register of equivalent document provided for that purpose, that each production batch satisfied the applicable provisions.

"> QP & QA Manager (m/f)

As Qualified Person (QP), you will be responsible for securing that each batch of medicinal products has been manufactured and checked in compliance with the laws in force in that Member State and in accordance with the requirements of the marketing authorization. Furthermore, you certify in a register of equivalent document provided for that purpose, that each production batch satisfied the applicable provisions.

QP & QA Manager (m/f)

Our client, Oxy Technical Gases, a leading technical, industrial and medical gas production company, is looking for an ideal candidate to fill in the position.

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Key Tasks & Responsibilities:
•  Building and implementing a documented Quality Management System and regular monitoring the compliance and effectiveness of the procedures and validations relating to regulated gases, informing the managers in case of deviations, and collaborating with them for implementation of the corrective actions
•  Ensuring that the changes in the processes relating to regulated gases comply with the provisions of the legislation
•  Ensuring the correct management of the documentary aspects relating to regulated gases as well as coordinating and carrying out the training of personnel on regulated gases
•  preparing and collaborating with the Managers in conducting audits and mock-recalls concerning medical gases, medical devices and food gases
•  Ensuring the effectiveness of the emergency plan relating to the withdrawal of the regulated gas from the market
•  Ensuring that the duties of the Quality Control function are properly met

Requirements:
•  University degree in Pharmacy or similar (e.g. medicine, veterinary medicine, chemistry, pharmaceutical chemistry and technology, biology)
•  2+ years of experience in Quality Assurance field, gained within the companies with license to manufacture medicinal products
•  Technical knowledge in the activities of qualitative analysis of medicinal products, quantitative analysis of medicinal active ingredients and testing and verification for the needs of quality assurance on medical products
•  Strong level of English literacy

If you would like to be part of an international company and are ready to take the initiative and responsibility, please send your CV and application letter in English. Full confidentiality is guaranteed.

Ivana Pršlja

+385 98 204 717

ivana.prslja@hill-international.com

Apply now