Mission :

• Supervise the quality assurance department and monitor activity
• Support and monitor production operations, quality control, maintenance, storage and distribution by applying Good Manufacturing Practices (BPF)
• Ensure all procedures lay down, validation and implementation
• Ensure that products are manufactured in accordance with good pharmaceutical manufacturing practices and guarantee the quality, safety and efficacy of products
• Ensure compliance with regulatory requirements for the production of drugs for human use
• Check production records and control documents, to be submitted to the pharmacist responsible for batch release
• Approve reprocessing protocols
• Ensure the implementation and monitoring of the validation master plan
• Approve protocols and validation report of the manufacturing process
• Approve cleaning validation protocols
• Approve equipment qualification protocols
• Ensure compliance with the equipment calibration schedule
• Ensure selection and qualification of suppliers of excipients

Profil recherché :

• Pharmacist. Master in biological science and quality engineering
• At least 3 years in Quality Assurance department, preferably with some experience in production or logistics
• Very good command of English
• Distinct management and leadership skills
• Problem solving competence
• Team spirit
• Taking initiatives

La création et l'exploitation d'un établissement pharmaceutique industriel, l'acquisition ou la prise en location de tout immeuble destiné à la fabrication des produits pharmaceutiques,