Junior Quality Manager - VIE Contract (W/M)

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTEthat since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTEthat applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address.

At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers.

Due to increase of complexity of business and of legal and Sanofi requirements, we need support for the management of a part of our quality system. This includes but is not limited to the management of Quality agreements, change controls, market batcth release for entire Sanofi portfolio, support in conduct of self-inspection, CAPA (corrective and preventative actions) follow up, risk management & complaints follow up for a part of Sanofi product portfolio. In addition, VIE will be involved in quality system activities which include set up or revision of processes & creation of associated SOPs (Standard Operating Procedures ) & trainings in accordance with legal requirements & Sanofi global documents.

As key responsibilities, you will have to manage in an autonomous manner:

• Market batch release
• Change control management (creation, follow up and closure)
• Product Quality Complaints management
• Risk Management
• Product Quality Review follow up
• Audit and CAPA (corrective and preventative actions) follow up
• Additional Quality System activities:
• Sanofi Global Documents review and implementation on Good Manufacture Practice (GMP) / Good Distribution Practice (GDP)related topics
• Setting or review of process and writing associated Standard Operating Procedure and ensure appropriate trainings

Requirements:

• Master’s degree in Pharmacy or equivalent
• Previous experience in a pharmaceutical environment with knowledge of EU GMP and GDP is a plus.
• Organized, fast learner with attention to details
• Ability with and interest on IT tools
• Ability to work under stress and time pressure
• Fluent English & French is a must, German or Italian would be a strong asset

Knowledge in:

• Chemical and pharmaceutical products
• Pharmaceutical environment
• International regulations, Good Manufacturing Practice (e.g EU GMP/GDP)
• Writing abilities
• Computer Applications
• Data bases

Skills:

• Communication
• Organisation
• Analysis/Synthesis
• Prioritisation
• Alert capacity
• Team Spirit
• Workload management

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.