Technical Group Leader – Flu Downstream (Night

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and  Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.

Sanofi’s global vaccines business unit partners with the public health, medical and scientific communities to improve access to life-protecting vaccines and increase vaccination coverage, while striving to develop new and improved vaccines to enhance health and well-being.

At Sanofi, we chase the miracles of science to improve people’s lives. We believe our cutting-edge science and manufacturing, fuelled by data and digital technologies, have the potential to transform the practice of medicine, turning the impossible into possible for millions of people.

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

• Schedule and coordinate daily/weekly work of group of technical staffinB
  200 as per area requirements.
• Check and review Records, SOP, logbooks/e-logbooks, BPRs/e-BPRs, and monitoring charts for completion and accuracy of all documents as per GMP guidelines.
• Ensure equipment is kept in good GMP condition (with preventive maintenance, validation and calibration).
• Order and ensure adequate chemicals, supplies, and spare parts for equipment.
• Train and ensure technical staff comply to GMP and SOP requirements.
• Facilitate daily meetings and report findings to management.
• Initiate and file deviations and lead investigations.
• Coordinate and support units within department (Upstream, Downstream, MWS) and other outside departments (Maintenance, Automation, QO test labs, etc.) and ensure timely completion of production activities.
• Perform other duties as assigned by Department Management throughout all stages of drug substance manufacturing.
• SupervisematerialhandlinginB
  200 Shipping, Receiving, and storage areas.

• Coordinate, oversee, and confirm technical staffs completion of SAP activities/transactions.
• Capacity planning and scheduling of materials and personnel.
• Create work orders for ETS/Maintenance.
• Maintain master recipes and production inventory.
• Create and maintain process orders with authorization to change orders upon demand.
• Ensure transactions are done in a timely, accurate manner.
• Oversee and support activities in required environmental monitoring systems.
• Ensure all data input is completed accurately and in a timely manner such as investigation data, LIMs, deviation filing, change request forms, etc.
• Perform activities in PCS and review data as required.

• Perform and delegate production calculations, measurements and release checks. Ensure each cleaning meets standards set in SOP, records, and in accordance with GMP.
• Observe in detail and report any process deficiencies, perform visual inspection of equipment for impurity and damage before and after cleaning.
• Perform and delegate utility sampling and environmental monitoring as required and ensure completion on schedule.
• Train technical staff on problem solving and troubleshooting as required.
• Ensure area is inspection ready. Knowledgeable to guide inspectors.
• Perform activities as needed based on access levels on equipment.

• Train and ensure technical staff comply with HSE requirements.
• Ensure operators are equipped and use proper PPE when performing tasks.
• Actively participate in activities done by HSE department and support HSE initiatives.
• Ensure operations are performed in an ergonomic way and elevate any potential hazards. Help develop proposed solutions.
• Ensure routine HSE checks and inspections are completed in a timely manner.
• Ensure cleaning chemicals and equipment are stored and used as per HSE…