Job Description

• Ensure compliance of the CPO organization with GxP legal and regulatory requirements, the Novartis Quality Manual and Policies & local GxP regulation.
• Contribute actively in the maintenance and update of the local Quality system and ensuring all Quality & Compliance KPIs are within target
• Manage and master all the internal IT tools necessary for the maintenance of good quality oversight.
• Contribute to maintain an updated local Master Documentation List and ensure all GxP documentation & SOPs are managed in a compliant way
• Ensure that all aspects of the handling, manufacturing and distribution of pharmaceutical products in the country comply with the requirements of the Novartis Quality Manual and Procedures and meet all relevant GxP regulatory and legislative requirements.
• Support the Quality department in the different projects (local/regional or global) contributing to upgrade the Quality level of the organization.
• Ensure that a local Quality System and SOP are in place for all GMP/GDP related activities and that compliance with GMP/GDP regulations is maintained through training and internal audits.
• Collaborate and Establish a good working relationship with the other departments, mainly SCM, RA, PV, GDQ, Medical, HR, Finance.
• Ensure that all drug products are released to the market in accordance with the registered specifications and with local/international regulations.
• Contribute to the handling of external inspections, complaints, recalls, counterfeits and product tampering according to the Novartis Corporate Quality Manual and local written procedures. Support / participate in NEM cases as required.
• Contribute to maintaining the training curriculum and follow-up GxP training at the CPO for all GxP related activities by defining, planning and supporting training activi-ties.

Commitment to Diversity & Inclusion :

• Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Minimum Requirements

•  Pharmacist diploma
•  French, English fluent in speaking and writing.
•  Min. 3 years experience in the pharmaceutical industry in a relevant field such as quality assurance, quality control, registration, production or a directly related area.

• Lieu de travail Maroc| Casablanca, Maroc
• Date d'expiration 16 Juillet
• Niveau de poste Confirmé / Expérimenté
• Secteur d'activité Distribution, Commerce
• Nombre de postes 01