Deputy Responsible Pharmacist

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argenx

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2008

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

Healthcare • Consulting • Biotechnology

argenx is a biotechnology company committed to improving the lives of patients through immunology innovation. The company focuses on developing novel antibody-based therapies to treat severe autoimmune diseases. Using a collaborative approach with pioneering scientists and academic partners, argenx accelerates the discovery of therapeutic antibodies that target specific disease pathways. The company's proprietary products, such as efgartigimod, are aimed at treating diseases where IgG antibodies are pathogenic. Argenx emphasizes innovation, science of collaboration, and patient-centric approaches in its mission to deliver life-changing medical solutions.

📋 Description

• Takes the role and responsibilities of the Responsible Pharmacist when he/she is out of the office • He/she organizes and supervises all the pharmaceutical operations of the company, and in particular the manufacture, advertising, information, pharmacovigilance, monitoring and withdrawal of batches, distribution, import and export of the medicines, products, objects as well as the corresponding storage operations • He/she shall ensure that the conditions of transport guarantee the proper preservation, integrity and safety of such medicines • He/she signs, after having read the file, the applications for marketing authorization submitted by the company • He/she participates in the development of the research and study program • He/she has authority over the delegated and deputy pharmacists; he/she gives his approval to their appointment and is consulted on their dismissal • He/she designates the interim delegate pharmacists • He/she shall inform the other managers of the company or body of any obstacle or limitation to the exercise of these powers • He/she shall take all necessary measures to ensure compliance with the obligations provided for in Articles R. 5124-48 and R. 5124-48-1 • In the case of medicinal products intended to be placed on the market in the European Union, he/she shall ensure that the safety devices referred to in Article R.5121-138-1 have been affixed to the packaging under the conditions laid down in Articles R. 5121-138-1 to R. 5121-138-4 • He/she shall notify the National Agency for the Safety of Medicines and Health Products of any placing on the national market of a medicinal product which he considers falsified within the meaning of the provisions of Article L. 5111-3, of which he is responsible for the manufacture, exploitation and distribution.

🎯 Requirements

• Experience in a pharmaceutical environment on similar activities (minimum 3 years) • He/she holds a European diploma in pharmacy or a recognised diploma from a third country (Article R 5132-30) • He/she is fluent in French (article R 5132-33) and English • He/she has a validated practical experience of 6 minimum months in quality control for companies with at least one manufacturing activity or importers or in pharmacovigilance and batch monitoring for companies with operator activities only.

🏖️ Benefits

• This job is eligible to participate in our short-term and long-term incentives program.